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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00634699
Other study ID # Éthic Committee, UQTR
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received March 6, 2008
Last updated June 25, 2011
Start date September 2006
Est. completion date September 2010

Study information

Verified date June 2011
Source Guy Hains Chiropractor
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to find the efficacy of treating the muscles in the inside (biceps,pronator teres) of the arm in order to eliminate the carpal tunnel syndrome .The authors hypothesise that eliminating the trigger points located in these muscles would diminish the symptoms associated with the carpal tunnel syndrome.


Description:

The carpal tunnel syndrome is a common condition which should treated by surgery only when conservative approaches has been tried.In the present trial the authors intend to find the effectiveness of treating the triggers points located in the biceps muscle, the pronator teres muscle and the biceps aponeurosis on the symptoms normally associated with the carpal tunnel syndrome.

The technique used in this trial will be ischemic compression(thumb tip pressure)on the trigger points located on the previous sites.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date September 2010
Est. primary completion date June 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Adults between 20 and 60 years old from the city and the surrounding Trois-Rivières with chronic carpal tunnel syndrome,

- Daily pain in the hand that lasted at least 3 months

Exclusion Criteria:

- History of upper limb or neck surgery,

- Pregnancy and systemic pathologies possibly related to carpal tunnel syndrome, such as hypothyroidism, diabetes and rheumatoid arthritis.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Active Comparator, ischemic compressions
Ischemic Compressions,3 times a week,5 weeks.

Locations

Country Name City State
Canada Guy Hains 2930 Côte Richelieu Trois-Rivières Quebec

Sponsors (1)

Lead Sponsor Collaborator
Guy Hains Chiropractor

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain,functional disabilities One year No
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