Acupuncture for Peripheral Neuropathy
Primary Purpose
Peripheral Neuropathy Grade 2 or Greater
Status
Terminated
Phase
Phase 2
Locations
Singapore
Study Type
Interventional
Intervention
acupuncture
Sponsored by
About this trial
This is an interventional treatment trial for Peripheral Neuropathy Grade 2 or Greater focused on measuring peripheral neuropathy, acupuncture, Bortezomib, Thalidomide
Eligibility Criteria
Inclusion Criteria:
- Age > 21 years and have a diagnosis of a plasma cell dyscrasia or lymphoma.
- Patients must have neuropathy greater or equal to 2 according to CTCAE v 3.0 scale in spite of adequate duration (at least 3 weeks) of previous treatment with Gabapentin or Pregabalin or are unable to tolerate these drugs. Patients receiving any of these drugs must remain on the same medications throughout the study period; however, minor adjustments in dosage are allowed.
3. The patient's current or previous treatment must include bortezomib or thalidomide
4. ECOG Performance Status of 0, 1, or 2
Exclusion Criteria:
- Local infection at or near the acupuncture site. (Although acupuncture is a minimally invasive procedure, patients will be excluded if there is an indication of active infection.)
- Thrombocytopenia (platelet counts < 50x 109/L) on the day of acupuncture session
- Deformities that could interfere with accurate acupuncture point location or out of energy pathway as defined by traditional acupuncture theory.
- Concurrent use of anticoagulation agents.
- Known coagulopathy and taking heparin (including low molecular weight heparin) or warfarin at any dose. Patients on aspirin or non-steroidal anti-inflammatories are allowed to participate.
- Persistent absolute neutrophil counts of < 1 x 109/L
- Active CNS disease.
- Patients having a cardiac pacemaker.
- Currently pregnant or lactating females.
- Severe diabetic neuropathy or neuropathy related to HIV.
- Previous acupuncture treatment for any indication within 30 days of enrollment.
Sites / Locations
- Singapore General Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
acupuncture treatment
Arm Description
Outcomes
Primary Outcome Measures
Improvement in peripheral neuropathy
Secondary Outcome Measures
Full Information
NCT ID
NCT01633281
First Posted
June 29, 2012
Last Updated
November 18, 2015
Sponsor
Singapore General Hospital
Collaborators
National Neuroscience Institute
1. Study Identification
Unique Protocol Identification Number
NCT01633281
Brief Title
Acupuncture for Peripheral Neuropathy
Official Title
A Study of Acupuncture for Bortezomib or Thalidomide -Induced Peripheral Neuropathy in Patients With Multiple Myeloma or Lymphoma
Study Type
Interventional
2. Study Status
Record Verification Date
November 2015
Overall Recruitment Status
Terminated
Why Stopped
poor recruitment and expiry of funding
Study Start Date
June 2012 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
June 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Singapore General Hospital
Collaborators
National Neuroscience Institute
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
A significant proportion (up to 60%) of myeloma patients treated with Bortezomib or thalidomide or both develop significant peripheral neuropathy (PN). Standard of care for this complication include drugs like gabapentin or pregabalin, which relieve symptoms only partially. PN of grade II or above mandates reduction in dose or frequency of Bortezomib or thalidomide, which may compromise treatment outcome. This clinical study explores whether, by intervening early in its course using acupuncture, progression of PN can be reversed, stabilized or retarded thereby allowing continuation of treatment on schedule.
Detailed Description
The acupuncture treatment will start after patients have received at least 3 weeks of Gabapentin or Pregabalin at adequate dose without improvement in PN
Two sessions of acupuncture per week, each of 30minutes duration, will be administered for a total of 10 sessions over 5 weeks. The needling will be done by the designated acupuncturist for all patients, delivered with electrical stimulation at a defined frequency.
A fixed set of acupoints will be applied which include both local and distant points, based on both symptoms of PN and classification of TCM syndrome. Some degree of flexibility with addition or reduction of acupoints is allowed based on clinical indication. The acupoints needled each session will be recorded.
Assessment of efficacy 4.1 Objective response : A complete neurological examination will be done at commencement of acupuncture and at end of acupuncture.
In addition, a full nerve conduction test will be done at beginning of acupuncture and at the end of 10 sessions of acupuncture.
4.2 Subjective assessment A quality of life questionnaire (FACT/GOG-NTX v4) will be filled in by patients at enrolment, commencement, at the 6th session and at the end of 10 sessions of acupuncture.
4.3 Scoring With both objective and subjective assessment, a Total Neuropathy Score can be calculated at each time point as a quantitative measurement of the severity of PN
5. Statistical considerations The statistical analysis specifies that a lower limit of the two-sided 90 percent confidence interval for the overall positive response that exceeded 10 percent would be considered to be evidence of significant efficacy of acupuncture in retarding Bortezomib or thalidomide induced PN. Allowing a confidence interval width of 30%, the sample size needed will be 34 patients. To allow for a 10% drop-out, we plan to recruit a total of 40 patients
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Neuropathy Grade 2 or Greater
Keywords
peripheral neuropathy, acupuncture, Bortezomib, Thalidomide
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Actual)
8. Arms, Groups, and Interventions
Arm Title
acupuncture treatment
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
acupuncture
Intervention Description
Ten sessions of acupuncture at 2x per week over 5 weeks will be given to patients. The acupuncture points include a standard set of obligatory points and additional points based on symptoms.
Primary Outcome Measure Information:
Title
Improvement in peripheral neuropathy
Time Frame
within the 5 weeks of acupuncture treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age > 21 years and have a diagnosis of a plasma cell dyscrasia or lymphoma.
Patients must have neuropathy greater or equal to 2 according to CTCAE v 3.0 scale in spite of adequate duration (at least 3 weeks) of previous treatment with Gabapentin or Pregabalin or are unable to tolerate these drugs. Patients receiving any of these drugs must remain on the same medications throughout the study period; however, minor adjustments in dosage are allowed.
3. The patient's current or previous treatment must include bortezomib or thalidomide
4. ECOG Performance Status of 0, 1, or 2
Exclusion Criteria:
Local infection at or near the acupuncture site. (Although acupuncture is a minimally invasive procedure, patients will be excluded if there is an indication of active infection.)
Thrombocytopenia (platelet counts < 50x 109/L) on the day of acupuncture session
Deformities that could interfere with accurate acupuncture point location or out of energy pathway as defined by traditional acupuncture theory.
Concurrent use of anticoagulation agents.
Known coagulopathy and taking heparin (including low molecular weight heparin) or warfarin at any dose. Patients on aspirin or non-steroidal anti-inflammatories are allowed to participate.
Persistent absolute neutrophil counts of < 1 x 109/L
Active CNS disease.
Patients having a cardiac pacemaker.
Currently pregnant or lactating females.
Severe diabetic neuropathy or neuropathy related to HIV.
Previous acupuncture treatment for any indication within 30 days of enrollment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yeh-Ching Linn, MBBS, MRCP
Organizational Affiliation
Singapore General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Singapore General Hospital
City
Singapore
ZIP/Postal Code
169608
Country
Singapore
12. IPD Sharing Statement
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