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NCT01317719

Prospective Biceps Study

Completed Last updated 18 September 2020
What this trial tests

trial testing Distal Biceps Re-Insertion Surgery in Biceps Tendon Rupture in 15 participants. Completed in 30 December 2013.

Timeline
14 January 2011
Primary endpoint
30 December 2013
30 December 2013

Quick facts

Lead sponsorWest Penn Allegheny Health System
StatusCompleted
Study typeOBSERVATIONAL
Enrollment15
Start date14 January 2011
Primary completion30 December 2013
Estimated completion30 December 2013
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

West Penn Allegheny Health System — full company profile →

Who can join

Adults 18 to 80, any sex, with Biceps Tendon Rupture. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary goal of this study is to determine if surgical repair of the distal biceps fully restores the supination strength of the forearm. Secondarily, the investigators want to examine the insertion site location of the tendon and determine if it correlates with the patients' functional outcome as determined by Disabilities of the Arm, Shoulder, and Hand (DASH), Visual Analog Pain Scale (VAPS), and isometric supination torque testing.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other West Penn Allegheny Health System trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01317719.

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