Effect of Distal Needling on Knee Pain Using Acupuncture Techniques

Sponsor
Hadassah Medical Organization (Other)
Overall Status
Completed
CT.gov ID
NCT01612663
Collaborator
(none)
70
1
4
36
1.9

Study Details

Study Description

Brief Summary

The purpose of this study is to test if specific therapeutic benefits of acupuncture are mostly attributable to contextual and psychosocial factors, such as patients' beliefs and expectations.The investigators propose using the 2 acupuncture methods, which refrains from inserting needles in the affected area, in order to evaluate the short-term and long-term efficacy of acupuncture in a clinical setting compared with placebo and compared with invasive needling that does not adhere to "correct" acupuncture rules.

Condition or Disease Intervention/Treatment Phase
  • Device: Pain relief by Acupuncture needle at non-specific site
  • Device: Acupuncture needle
  • Device: Acupuncture needle
  • Device: Acupuncture needle
N/A

Detailed Description

The main novel features of this study:
  1. First aim to assess the effect of distal needling on knee pain

  2. Second aim to directly compare two acupuncture techniques, placebo, needling at "wrong" places and "correct" needling for knee pain

Advantages of the study compared to published data:
  1. Distal needling - enables assessment of range of motion (ROM) and pain level during needling.

  2. Both acupuncture systems rely on minimal questioning, which simplifies the patient-practitioner interactions.

  3. Exploratory studies in the clinic of DP show that it is possible to distinguish between "correct" and "incorrect" needling, at least in the short term. Long term effects have not been assessed yet.

Study Design

Study Type:
Interventional
Actual Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Basic Science
Official Title:
Comparison of Different Acupuncture Methods on Knee Pain
Study Start Date :
Jun 1, 2012
Actual Primary Completion Date :
Jun 1, 2014
Actual Study Completion Date :
Jun 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: deep needle non-site specific

Device: Pain relief by Acupuncture needle at non-specific site

Active Comparator: contralateral elbow to the knee pain

Device: Acupuncture needle

Active Comparator: Energy of Living Systems Needling

Device: Acupuncture needle

Placebo Comparator: Sham acupuncture

Device: Acupuncture needle

Outcome Measures

Primary Outcome Measures

  1. Effect of Distal Needling on Knee Pain Using Acupuncture Techniques [2 years]

    Effect of Distal Needling on Knee Pain Using 4 different Acupuncture Techniques by: Pain measurement by Visual Analogue Scale (VAS) Range of motion (ROM)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult patients (> 18 years old), suffering chronic stable pain score >40 mm on 100 mm VAS of the knee due to patellar tendonitis.

  • Patients have had X-rays or other tests confirming they are not candidates for surgery nor are scheduled for steroid injections or hyaluronic acid injections within 8 weeks from the beginning of the study.

  • Adult patients (> 18 years old), two weeks after ACL reconstruction surgery (with or without meniscal involvement), with pain score >40 mm on 100 mm VAS of the knee (all patients at this stage have significant ROM limitation).

Exclusion Criteria:
  • Patient refusal

  • Soldiers

  • Pregnancy

  • Morbid obesity

  • Diabetes

  • Peripheral vascular disease

  • Lower limb neurological deficit (such as multiple sclerosis, nerve palsy), other serious co-morbidity (including severe back pain or hip pain)

  • A history of prolonged or current steroid use

  • Received hyaluronic acid injections within the previous 3 months

  • Have needle phobia or allergy to sticking plaster.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hadassah Medical Organization Jerusalem Please Select Israel 91120

Sponsors and Collaborators

  • Hadassah Medical Organization

Investigators

  • Principal Investigator: Elyad Davidson, MD, Hadassah Medical Organization

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Elyad Davidson, PI Head Pain Unit, Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT01612663
Other Study ID Numbers:
  • 007212-HNO-CTIL
First Posted:
Jun 6, 2012
Last Update Posted:
Mar 22, 2022
Last Verified:
Mar 1, 2022
Keywords provided by Elyad Davidson, PI Head Pain Unit, Hadassah Medical Organization
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 22, 2022