Scapholunate Ligament Reconstruction Using Modified Flexor Carpi Radialis Tenodesis

NCT07667114 | Recruiting

• 1 other identifier: BB 112/26
• Study Type: observational
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

Retrospective study of patients who underwent a modified flexor carpi radialis (FCR) tenodesis for scapholunate ligament injury at Waldfriede Hospital during the period 2016-2026. Primary outcome: Functionality of the operated wrist measured using the validated DASH questionnaire.

Conditions

Scapholunate Dissociation; Scapholunate Ligament Rupture

Keywords

Scapholunate ligament; modified flexor carpi radialis (FCR) tenodesis; wrist

Outcome Measures

Primary Outcomes (1)

• DISABILITIES OF THE ARM, SHOULDER AND HAND (DASH) questionnaire

  DISABILITIES OF THE ARM, SHOULDER AND HAND; This questionnaire asks about symptoms as well as the ability to do certain activities regarding the upper limbs. Measure uses a 0 to 100 scoring scale, where lower scores (close to 0) represent no disability, and higher scores (close to 100) indicate maximum severity or inability to perform.

  At enrollment

Interventions

modified flexor carpi radialis tenodesis PROCEDURE

Flexor carpi radialis (FCR) tenodesis for the reconstruction of the dorsal scapholunate (SL) ligament and the dorsal intercarpal ligament (DICL)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Participation in the study is offered to all eligible patients who underwent a modified flexor carpi radialis (FCR) tenodesis for an SL ligament injury at Waldfriede Hospital between 2016 and 2026.

You may qualify if:

• Age: ≥ 18 years
• Capable of providing informed consent independently
• Availability of written informed consent for the study

You may not qualify if:

• Active malignant disease
• Pregnancy at the time of the examination
• Presence of SLAC arthritis
• Lack of capacity to provide independent consent

Sponsors & Collaborators

• Waldfriede Hospital: lead

Study Sites (1)

Waldfriede Hospital

Berlin, State of Berlin, 14163, Germany

RECRUITING

Central Study Contacts

Markus Bock, Dr. med.

CONTACT

+493081810200; m.bock@waldfriede.de

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 18, 2026
• First Posted: June 24, 2026
• Study Start: July 1, 2026
• Primary Completion (Estimated): January 31, 2027
• Study Completion (Estimated): May 31, 2027
• Last Updated: July 2, 2026

Record last verified: 2026-07

Data Sharing

• IPD Sharing: Will not share

Locations

DE (1)