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Scapholunate Ligament Reconstruction Using Modified Flexor Carpi Radialis Tenodesis

Clinical Outcomes of Scapholunate Ligament Reconstruction Using Modified Flexor Carpi Radialis Tenodesis - A Retrospective Study From 2016-2026

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07667114
Enrollment
100
Registered
2026-06-24
Start date
2026-07-01
Completion date
2027-05-31
Last updated
2026-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Scapholunate Dissociation, Scapholunate Ligament Rupture

Keywords

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

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.

Interventions

PROCEDUREmodified flexor carpi radialis tenodesis

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

Sponsors

Waldfriede Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
DISABILITIES OF THE ARM, SHOULDER AND HAND (DASH) questionnaireAt enrollmentDISABILITIES 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.

Countries

Germany

Contacts

CONTACTMarkus Bock, Dr. med.
m.bock@waldfriede.de+493081810200

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 3, 2026