Clinical Trial: Delto-Tricipital Compression Syndrome: Treated With Injection of Dextrose

Study Status: Recruiting
Recruit Status: Unknown status
Study Type: Interventional

Official Title: Delto-Tricipital Compression Syndrome: A Randomized Treatment Comparison Trial of Dextrose Injection Versus Physical Therapy.

Brief Summary: The posterior antebrachial cutaneous nerve (PACN) can be compressed between the deltoid and triceps, with resultant pain and dysfunction. The active treatment for this study will be injection of the point of compression and along the painful course of the sensory nerve with 5% dextrose. The control treatment will be physical therapy.

Detailed Summary:

The PACN is a purely sensory nerve that originates in the midforearm, courses anterior to the lateral epicondyle, and travels proximally until it dives between the posterior portion of the V shaped insertion of the deltoid and the external? insertion of the triceps, whereupon it joins with the radial nerve.

A proposed pathological explanation is that repetitive co-contraction produces irritation and compression of the nerve at the delto-tricipital (D-T) fascial penetration point. Clinically the patient experiences pain localized to that compression point, and traveling distally along the course of some or all of the posterior femoral cutaneous nerve.

Perineural injection of dextrose has been previously reported for therapeutic use in chronic pain associated with Achilles tendinopathy. Empirically,injection of D5W with a small needle along the course of the PACN and at the D-T penetrator has been found to resolve both pain and dysfunction (describe dysfunction).

Participants will be randomly assigned to either 1 month of physical therapy or to 0,1,2 and 3 week injection of D5W. The use of standardized measurement tools for pain (0-10 numerical rating scale) and function (Quick DASH) will be utilized to determine baseline status and status at 1 month. At 1 month, subjects receiving therapy will be allowed to cross over to injection treatment and all participants will receive as needed treatment until the 1 year period of follow-up. Thus only 1 month data is randomized but long term data will be gathered.


Sponsor: Universidad Abierta Interamericana

Current Primary Outcome: NRS Pain (0-10 Numerical Rating Scale) [ Time Frame: Time 0 and 1 month ]

0-10 Numerical Rating Scale for pain.


Original Primary Outcome: Same as current

Current Secondary Outcome: Quick Dash Score [ Time Frame: Time 0 and 1 month ]

Validated shortened version of Disabilities of Arm Shoulder and Hand score.


Original Secondary Outcome: Same as current

Information By: Universidad Abierta Interamericana

Dates:
Date Received: December 17, 2014
Date Started: January 2015
Date Completion: January 2017
Last Updated: March 13, 2015
Last Verified: March 2015