- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03449667
Cryoanalgesia to Treat Post-Amputation Phantom Limb Pain: A Department of Defense Funded Multicenter Study
Cryoanalgesia to Treat Post-Amputation Phantom Limb Pain: A Multicenter, Randomized, Double-Masked, Placebo-Controlled, Definitive Human Subjects Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Subjects will be asked to make no changes to their analgesic regimen for at least 1 month prior to the cryoneurolysis procedure and continuing for 4 months until the measurement of the primary end point-for the duration of the study, all patients will be allowed to continue their pre-intervention analgesics. All subjects will have a peripheral intravenous catheter inserted, standard noninvasive monitors applied, and oxygen administered via a facemask or nasal cannula. Midazolam and fentanyl (IV) will be titrated for patient comfort. The specific nerves targeted will be the sciatic and femoral (or their distal branches). The potential cryoneurolysis sites will be cleansed with chlorhexidine gluconate and isopropyl alcohol. The target nerves will be identified in a transverse cross-sectional (short axis) view using ultrasound. A Tuohy-tip needle will be inserted beneath the ultrasound transducer and directed until the needle tip is immediately adjacent to the target nerve. Local anesthetic (1-3 mL, lidocaine 2%) will be injected. This will be repeated for the femoral nerve. Within 20 minutes of the second injection, the subject's limb pain level will be evaluated on the 0-10 NRS and if higher than at baseline prior to injection, the subject will NOT continue with treatment and their participation in the study will terminate upon discharge.
Treatment group assignment (randomization). Remaining subjects will be allocated to one of two possible treatments:
- cryoneurolysis
- sham cryoneurolysis (placebo control)
Randomization will be computer-generated and stratified by enrolling institution in randomly chosen block sizes. Cryoneurolysis probes are available that either (1) pass nitrous oxide to the tip inducing freezing temperatures; or, (2) vent the nitrous oxide at the base of the probe so that no gas reaches the probe tip, resulting in no temperature change (PainBlocker, Epimed, Farmers Branch, Texas). Importantly, these probes are indistinguishable in appearance. Unmasking will not occur until statistical analysis is complete.
Intervention. The potential cryoneurolysis sites will be again cleansed with chlorhexidine gluconate and isopropyl alcohol. With the same ultrasound transducer used to previously administer local anesthetic, the target nerve will again be identified in a transverse cross-sectional (short axis) view at or distal to the deposition of local anesthetic. A cryoneurolysis device (PainBlocker, Epimed, Farmers Branch, Texas) will be inserted with the appropriate randomization-designated probe (either active or sham/placebo) and nitrous oxide. The cryoneurolysis device will be triggered using 3 cycles of 2-minute gas activation (active or sham) separated by 1-minute defrost periods. The process will be repeated with the same treatment probe for the femoral nerve (e.g., both nerves will receive either active cryoneurolysis or sham/placebo, and not a mix of the two possible treatments).
Optional crossover treatment. Four to 6 months following the initial treatment, subjects may return for an optional repeated intervention procedure ("crossover") with the alternative treatment (either active cryoneurolysis or sham/placebo), again in a double-masked fashion using the same protocol as described for the initial intervention. The crossover treatment is not required for study participation, as the primary analyses will include a parallel study design for the initial intervention evaluated prior to any crossover treatment. This crossover will not affect the primary analyses, which will involve a parallel group study design and investigate the effects of cryoneurolysis within 4 months of the initial intervention.
Outcome measurements (endpoints). The primary end point will be the difference in average daily phantom pain intensity at baseline and 4 months following the initial intervention (measured with the NRS as part of the Brief Pain Inventory). The primary analyses will compare the two treatments (inter-subject comparisons) during the initial treatment period in which half of the subjects will receive active cryoneurolysis and the other half a sham/placebo treatment. Endpoints will be evaluated at baseline and post-treatment (Day 0), Days 1 and 7; and Months 1, 2, 3, 4, and 12. These same time points through Month 4 will be evaluated following the optional second (crossover) treatment.
Data collection. The questionnaires for all subjects-regardless of enrolling center-will be administered by telephone from the University of California San Diego by research coordinators specifically trained in these instruments' application, minimizing inter-rater discordance. Staff masked to treatment group assignment will perform all assessments.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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California
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Palo Alto, California, United States, 94304
- Veterans Affairs Palo Alto Health Care System
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San Diego, California, United States, 92134
- Naval Medical Center San Diego (NMCSD)
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San Diego, California, United States, 92103
- University California San Diego
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Florida
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Gainesville, Florida, United States, 32610
- University of Florida
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Maryland
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Bethesda, Maryland, United States, 20889
- Walter Reed National Military Medical Center
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Ohio
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Cleveland, Ohio, United States, 44195
- Cleveland Clinic
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adult patients of at least 18 years of age
- with a lower limb traumatic or surgical amputation at least 12 weeks prior to enrollment distal to the hip (femoral head remaining)
- who experience at least moderate phantom limb pain-defined as a 3 or higher on the Numeric Rating Scale (NRS; 0-10, 0= no pain; 10=worst imaginable pain)-at least daily for the previous 2 months.
- accepting of a cryoneurolysis procedure
- willing to avoid both changes to their analgesic regimen as well as elective surgical procedures from 1 month prior to and at least 4 months following the initial cryoneurolysis procedure.
Exclusion Criteria:
- allergy to amide local anesthetics
- pregnancy
- incarceration
- inability to communicate with the investigators
- morbid obesity (body mass index > 40 kg/m2)
- possessing any contraindication specific to cryoneurolysis such as a localized infection at the treatment site, cryoglobulinemia, cold urticaria and Reynaud's Syndrome.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Cryoneurolysis first, then optional sham crossover treatment
Initial treatment: Cryoneurolysis of the femoral and sciatic nerves (or their distal counterparts) in the residual limb: The cryoneurolysis device will be triggered using 3 cycles of 2-minute gas activation separated by 1-minute defrost periods. For active probes, the nitrous oxide will be deployed to the tip where a drop in temperature to -70°C will result in cryoneurolysis. Optional sham crossover treatment: Sham cryoneurolysis of the femoral and sciatic nerves (or their distal counterparts) in the residual limb: The cryoneurolysis device will be triggered using 3 cycles of 2-minute gas activation separated by 1-minute defrost periods. However, for sham probes, the nitrous oxide is not deployed to the tip and therefore there is no drop in temperature resulting in cryoneurolysis. |
Cryoneurolysis of the femoral and sciatic nerves (or their distal counterparts) in the residual limb: The cryoneurolysis device will be triggered using 3 cycles of 2-minute gas activation separated by 1-minute defrost periods.
For active probes, the nitrous oxide will be deployed to the tip where a drop in temperature to -70°C will result in cryoneurolysis.
Other Names:
Sham cryoneurolysis of the femoral and sciatic nerves (or their distal counterparts) in the residual limb: The cryoneurolysis device will be triggered using 3 cycles of 2-minute gas activation separated by 1-minute defrost periods.
However, for sham probes, the nitrous oxide is not deployed to the tip and therefore there is no drop in temperature resulting in cryoneurolysis.
Other Names:
|
Sham Comparator: Sham Comparator first, then optional cryoneurolysis treatment
Initial treatment: Sham cryoneurolysis of the femoral and sciatic nerves (or their distal counterparts) in the residual limb: The cryoneurolysis device will be triggered using 3 cycles of 2-minute gas activation separated by 1-minute defrost periods. However, for sham probes, the nitrous oxide is not deployed to the tip and therefore there is no drop in temperature resulting in cryoneurolysis. Optional cryoneurolysis treatment: Cryoneurolysis of the femoral and sciatic nerves (or their distal counterparts) in the residual limb: The cryoneurolysis device will be triggered using 3 cycles of 2-minute gas activation separated by 1-minute defrost periods. For active probes, the nitrous oxide will be deployed to the tip where a drop in temperature to -70°C will result in cryoneurolysis. |
Cryoneurolysis of the femoral and sciatic nerves (or their distal counterparts) in the residual limb: The cryoneurolysis device will be triggered using 3 cycles of 2-minute gas activation separated by 1-minute defrost periods.
For active probes, the nitrous oxide will be deployed to the tip where a drop in temperature to -70°C will result in cryoneurolysis.
Other Names:
Sham cryoneurolysis of the femoral and sciatic nerves (or their distal counterparts) in the residual limb: The cryoneurolysis device will be triggered using 3 cycles of 2-minute gas activation separated by 1-minute defrost periods.
However, for sham probes, the nitrous oxide is not deployed to the tip and therefore there is no drop in temperature resulting in cryoneurolysis.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change From Baseline in Average Daily Phantom Pain Intensity
Time Frame: Baseline and 4 months later (difference between the two is the primary end point)
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The difference in average daily phantom pain intensity at baseline and 4 months following the initial intervention (measured with the numeric rating scale as part of the Brief Pain Inventory with a minimum value of 0 and maximum value of 10, 0=no pain and 10=worst imaginable pain)
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Baseline and 4 months later (difference between the two is the primary end point)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Average Daily Phantom Pain Intensity
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
The average daily phantom pain intensity at between 1 day and 12 months following the initial intervention (measured with the numeric rating scale as part of the Brief Pain Inventory with a minimum value of 0 and maximum value of 10, 0=no pain and 10=worst imaginable pain) To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Worst Daily Phantom Pain Intensity
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
The worst daily phantom pain intensity at between 1 day and 12 months following the initial intervention (measured with the numeric rating scale as part of the Brief Pain Inventory with a minimum value of 0 and maximum value of 10, 0=no pain and 10=worst imaginable pain). The worst pain is the maximum experienced in the previous 72 hour period (except day 1 which is the previous 24 hour period). To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Residual Limb Pain, Average
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Residual limb pain will be assessed using a Numeric Rating Scale which is a highly-sensitive measure of pain intensity with numbers ranging from 0 to 10, with zero equivalent to no pain and 10 equivalent to the worst imaginable pain. To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Residual Limb Pain, Worst
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Residual limb pain will be assessed using a Numeric Rating Scale which is a highly-sensitive measure of pain intensity with numbers ranging from 0 to 10, with zero equivalent to no pain and 10 equivalent to the worst imaginable pain. The worst pain is the maximum experienced over the previous 72 hours (24 hours for Day 1). To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Patient Global Impression of Change
Time Frame: Endpoints will be evaluated on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
The Patient Global Impression of Change Scale is a 7-point ordinal scale requiring the subject to rate the current severity of their global situation as it relates to phantom limb pain (as defined by each individual) compared to their baseline. This scale has the words "very much worse" to the left by the number one, and "very much improved" to the right, adjacent to the number seven. The words "no change" are in the middle of the scale above the number four. The Patient Global Impression of Change Scale has been validated in over ten prospective trials, including studies specifically involving peripheral neuropathy To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially f |
Endpoints will be evaluated on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Brief Pain Inventory Interference Subscale
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
The Brief Pain Inventory (interference sub scale) is an instrument that measures the interference with physical and emotional functioning using a 0-10 scale (0 = no interference; 10 = complete interference). The seven interference questions involve general activity, mood, walking ability, normal work activities (both inside and outside of the home), relationships, sleep, and enjoyment of life. The seven functioning questions can be added to produce an interference subscale (0-70). A higher score reveals more interference with physical and emotional functioning. To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Beck Depression Inventory
Time Frame: At baseline, 4 months after the initial and crossover treatments as well as 12 months after the initial treatment
|
The Beck Depression Inventory is a 21-item instrument that measures characteristic symptoms and signs of depression, requires only a 5th grade comprehension level to adequately understand the questions, and demonstrates a high internal consistency (0.73-0.92, mean of 0.86), reliability and validity. Each of the 21 factors is rated on a 0-3 scale, and then summed to produce the total score of 0-63. Mild, moderate, and severe depression is defined with scores of 10-18, 19-29, and 30-63, respectively. To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Month 4 provides the results for those receiving cryoneurolysis while "crossover" Month 4 provides the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
At baseline, 4 months after the initial and crossover treatments as well as 12 months after the initial treatment
|
Phantom Limb Pain Frequency
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Pain perceived to emanate from part of the injured limb that no longer exists. The frequency is the number of times this is experienced in the previous 72 hours. To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Phantom Limb Pain Duration
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Pain perceived to emanate from part of the injured limb that no longer exists. The duration is the average number of hours that each occurrence is experienced in the previous 72 hours. To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Non-painful Phantom Sensations Frequency
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Sensations that feel to emanate from the missing limb, but are not described as pain. The frequency is the number of times this is experienced in the previous 72 hours. To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Non-painful Phantom Sensations Duration
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Sensations that feel to emanate from the missing limb, but are not described as pain. The duration is the average duration of each experience over the previous 72 hours. To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Residual Limb Pain Frequency
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Pain that originates from a part of the injured limb that remains intact. The frequency is the number of times residual pain is experienced in the previous 72 hours. To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Residual Limb Pain Duration
Time Frame: Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Pain that originates from a part of the injured limb that remains intact. The duration is the average number of hours that residual pain was experienced each episode in the previous 72 hours. To read the results: for the group that received cryoneurolysis initially followed by sham for the crossover treatment, "initial" Days 1 - Month 4 provide the results for those receiving cryoneurolysis while "crossover" Days 1 - Month 4 provide the results for those receiving sham treatment. This is reversed for the other treatment group that received sham initially followed by cryoneurolysis for the crossover treatment. |
Endpoints will be evaluated at baseline and on Days 1 and 7; and Months 1, 2, 3, and 4 after both the initial and subsequently the crossover treatments; and 12 months after the initial treatment
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Brian M Ilfeld, MD, MS, University California San Diego Department of Anesthesiology
- Study Director: Rodney Gabriel, MD, MAS, University California San Diego Department of Anesthesiology
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CRYO for Phantom Pain (DoD)
- W81XWH-17-2-0051 (Other Grant/Funding Number: Peer Reviewed Medical Research Program (PRMRP))
- PR160263 (Other Grant/Funding Number: Department of Defense Congressionally Directed Medical Research Programs)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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