Scapholunate Ligament Injury Treated with Modified FCR Tenodesis at Waldfriede Hospital

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a retrospective observational study of adults who had a modified FCR tenodesis for scapholunate ligament injury at Waldfriede Hospital between 2016 and 2026. The main outcome is wrist function measured by the DASH questionnaire. Data are drawn from patients who could provide informed consent and who did not have active cancer, pregnancy, SLAC arthritis, or cognitive impairment that would prevent consent. No external comparison group or interventional protocol is described beyond the surgical procedure. The study aims to summarize functional outcomes after this specific surgical approach in a real-world setting.

Why it matters

Who can join: the full rules

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

Where it's running

• Waldfriede Hospital
  Berlin, State of Berlin, Germany Recruiting

Study contacts

• Study coordinator: Markus Bock, Dr. med.
• Email: m.bock@waldfriede.de
• Phone: +493081810200

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.