- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02058836
Botulinum Toxin for the Management of Chronic Orchialgia
August 7, 2018 updated by: Wake Forest University Health Sciences
The purpose of this research study is to determine if Botox injections will provide relief from chronic testicular pain.
In the study, the spermatic cord of particpants will be injected with either Botox or a placebo of saline.
Botox is currently used to treat other urological conditions like overactive bladder and lower urinary tract problems.
For these conditions, Botox works by relaxing muscles in the affected areas.
The investigators believe that Botox will act similarly in the treatment chronic testicular pain.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
8
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
North Carolina
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Winston-Salem, North Carolina, United States, 27103
- Wake Forest School of Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Clinical diagnosis of chronic testicular pain (orchialgia)
Exclusion Criteria:
- Active infection of urinary tract (UTI)
- Active infection of the scrotal skin of the affected side
- Bilateral orchiectomy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Botox Injection
The participant will be given an injection of Botox along the spermatic cord under ultrasound guidance.
Before drug administration, a nerve block using bupivacaine will be completed to numb the area for treatment.
This will be a 10 mL injection done one time at the initial patient visit.
|
One-time injection of 100 Units of Botox in 10 mL of saline.
The 10 mL injection will be distributed in 4 areas around the spermatic cord and testicle of the affected side with 2.5 mL being injected at each area.
Other Names:
|
|
Placebo Comparator: Saline Injection
The patient will receive an inactive injection of normal saline along the spermatic cord under ultrasound guidance.
This will be a 10 ml injection done once at the initial visit.
Before the injection of saline, a spermatic cord block using bupivacaine will be completed to numb the area for treatment.
|
One-time injection of 10 mL of 0.9% sodium chloride (normal saline) solution.
The 10 mL injection will be distributed in 4 areas around the spermatic cord and testicle of the affected side with 2.5 mL being injected at each area.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analog Scale for Pain Score
Time Frame: Baseline and 1 Week Post Injection
|
Visual Analog Scale for Pain Score (VAS).
It measures a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms such as pain.
VAS is a straight horizontal line of fixed length, usually 100 mm.
The patient marks on the line the point that they feel represents their perception of their current state.The VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patient marks.
The score range is from 0-100.
Lower scores denotes better outcomes.
|
Baseline and 1 Week Post Injection
|
|
Visual Analog Scale for Pain Score
Time Frame: 1 month
|
Visual Analog Scale for Pain Score.
It measures a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms such as pain.
VAS is a straight horizontal line of fixed length, usually 100 mm.
The patient marks on the line the point that they feel represents their perception of their current state.The VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patient marks.
The score range is from 0-100.
Lower scores denotes better outcomes.
|
1 month
|
|
Visual Analog Scale for Pain Score
Time Frame: 3 months
|
Visual Analog Scale for Pain Score.
It measures a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms such as pain.
VAS is a straight horizontal line of fixed length, usually 100 mm.
The patient marks on the line the point that they feel represents their perception of their current state.The VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patient marks.
The score range is from 0-100.
Lower scores denotes better outcomes.
|
3 months
|
|
Visual Analog Scale for Pain Score
Time Frame: 6 months
|
Visual Analog Scale for Pain score.
It measures a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms such as pain.
VAS is a straight horizontal line of fixed length, usually 100 mm.
The patient marks on the line the point that they feel represents their perception of their current state.The VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patient marks.
The score range is from 0-100.
Lower scores denotes better outcomes.
|
6 months
|
|
Quality of Life Questionnaire Score
Time Frame: 1 week
|
Quality of Life Questionnaire Score (QOL).
To assess the QOL, a short form-36 (SF-36) was used.
SF-36 is a set of generic, coherent, and easily administered quality-of-life measures.
The SF-36 consists of eight items, which are the weighted sums of the questions in their section.
The eight items are: vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, and mental health.
Each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively.
Scores represent the percentage of total possible score achieved.
Items in the same scale are averaged together to create the 8 scale scores.
Scale scores represent the average for all items in the scale that the respondent answered.
Higher scores denotes better outcomes.
|
1 week
|
|
Quality of Life Questionnaire Score
Time Frame: 1 month
|
Quality of Life Questionnaire Score.
To assess the QOL, a SF-36 was used.
SF-36 is a set of generic, coherent, and easily administered quality-of-life measures.
The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section.
The eight sections are: vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, and mental health.
Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight.
The score range is 0-100 and higher scores denotes better outcomes.
|
1 month
|
|
Quality of Life Questionnaire Score
Time Frame: 3 months
|
Quality of Life Questionnaire Score (QOL).
To assess the QOL, a short form-36 (SF-36) was used.
SF-36 is a set of generic, coherent, and easily administered quality-of-life measures.
The SF-36 consists of eight items, which are the weighted sums of the questions in their section.
The eight items are: vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, and mental health.
Each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively.
Scores represent the percentage of total possible score achieved.
Items in the same scale are averaged together to create the 8 scale scores.
Scale scores represent the average for all items in the scale that the respondent answered.
Higher scores denotes better outcomes.
|
3 months
|
|
Quality of Life Questionnaire Score
Time Frame: 6 months
|
Quality of Life Questionnaire Score (QOL).
To assess the QOL, a short form-36 (SF-36) was used.
SF-36 is a set of generic, coherent, and easily administered quality-of-life measures.
The SF-36 consists of eight items, which are the weighted sums of the questions in their section.
The eight items are: vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, and mental health.
Each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively.
Scores represent the percentage of total possible score achieved.
Items in the same scale are averaged together to create the 8 scale scores.
Scale scores represent the average for all items in the scale that the respondent answered.
Higher scores denotes better outcomes.
|
6 months
|
|
Units of Analgesics Used for Testicular Pain
Time Frame: 1 week
|
Change from Baseline in Units of Analgesics Used for Testicular Pain
|
1 week
|
|
Units of Analgesics Used for Testicular Pain
Time Frame: 1 month
|
Change from Baseline in Units of Analgesics Used for Testicular Pain
|
1 month
|
|
Units of Analgesics Used for Testicular Pain
Time Frame: 3 months
|
Change from Baseline in Units of Analgesics Used for Testicular Pain
|
3 months
|
|
Units of Analgesics Used for Testicular Pain
Time Frame: 6 months
|
Change from Baseline in Units of Analgesics Used for Testicular Pain
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Ryan P Terlecki, MD, Wake Forest University Health Sciences
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2014
Primary Completion (Actual)
October 18, 2016
Study Completion (Actual)
October 18, 2016
Study Registration Dates
First Submitted
February 5, 2014
First Submitted That Met QC Criteria
February 7, 2014
First Posted (Estimate)
February 10, 2014
Study Record Updates
Last Update Posted (Actual)
September 5, 2018
Last Update Submitted That Met QC Criteria
August 7, 2018
Last Verified
August 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB00023188
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Yes
Studies a U.S. FDA-regulated device product
No
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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