- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00136669
Acupuncture For Pancreatic Cancer Pain
Acupuncture For Pancreatic Cancer Pain: A Randomized Phase III Study
Pain is a common problem in patients with pancreatic cancer. Some patients suffer from pain despite medication. We, the researchers at Memorial Sloan-Kettering Cancer Center, are conducting a Phase III study to determine the effects of acupuncture on pain in patients with pancreatic cancer. The purpose of a Phase III study is to determine whether or not a treatment is helpful. This study will include about 60 patients.
Acupuncture is the insertion of very fine needles into the skin to treat symptoms. In recent years, researchers have found evidence that acupuncture is useful in treating a variety of conditions, including headache, nausea, and pain.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The main aim of this pancreatic cancer pain trial is to determine the effects of a single, practitioner-given acupuncture treatment followed by semi-permanent acupuncture studs. Our primary endpoint is subjective; therefore, a placebo control will be applied with patients blinded to treatment allocation.
In clinical practice, acupuncturists individualize treatment: two patients with a similar conventional diagnosis may receive different point prescriptions depending on the acupuncture differential diagnosis. Randomized trials of acupuncture can either prescribe a fixed treatment formula in terms of the number of sessions and points to be used, or allow practitioners to exercise clinical judgment in individualizing care. There has been considerable debate in the methodological literature about the merits of each approach. The use of a fixed treatment schedule increases the reproducibility of the findings but is said, by practitioners, to generally reduce treatment effectiveness. In this trial, we have developed an approach that allows practitioners to individualize treatments in a manner that allows exact replication, by specifying particular point locations to be used depending on the sites where a patient experiences pain. Point locations for this and for all of our acupuncture studies are determined by our licensed, credentialled acupuncturists.
Following accrual of the initial 10-15 patients, we will review treatment compliance, blinding and accrual. Adjustments will be made to deal with compliance issues, to facilitate placebo blinding, or deal with recruitment problems for the remainder of the study.
Study Type
Enrollment
Phase
- Phase 3
Contacts and Locations
Study Locations
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New York
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New York, New York, United States, 10021
- Memorial Sloan-Kettering Cancer Center
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Diagnosis of pancreatic adenocarcinoma.
- First baseline current pain score of 3 or above on a 0 - 10 numerical rating scale.
- In the opinion of the treating physician or a medically qualified investigator, the patient's pain syndrome is the result of underlying cancer.
- Patient OR caregiver must be willing and able to apply pressure to each point using small circular movements with the fingers twice per day.
Exclusion Criteria:
- Primary cause of pain is procedural (e.g. postoperative pain).
- Acupuncture treatment in the past six weeks. Patients should not receive acupuncture during the one week period of the study.
- Neutropenia defined as absolute neutrophil count (ANC) <1000/microliter.
- Cardiac conditions constituting high or moderate risk of endocarditis as defined by the American Heart Association criteria.
- Patient contraindicated for phlebotomy, as phlebotomy needles are much larger than acupuncture needles.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
To determine whether acupuncture reduces pain in pancreatic cancer patients more effectively than placebo
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To determine the duration of acupuncture effects
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Collaborators and Investigators
Investigators
- Principal Investigator: Barrie R. Cassileth, Ph.D., Memorial Sloan Kettering Cancer Center
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Study Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 03-106
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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