CompletedNot Applicable

Randomized Trial of Active vs Passive Splinting for Extensor Tendon Injuries in Zones IV to VI

Spain30 participantsStarted 2020-07-01

Plain-language summary

This study compares two methods of post-operative immobilization after surgical repair (tenorrhaphy) of extensor tendons in the fingers. Patients were randomly assigned to receive either a standard plaster splint or an alternative splinting method that allows controlled finger movement (ICAMS). The main goal was to determine which method leads to better recovery in terms of finger mobility, grip strength, pain, and patient comfort.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Adults aged 18 years or older * Patients from the CHUVI Health Area * Diagnosed with an acute, single, complete extensor tendon laceration in zones IV, V, or VI of the long fingers * Treated with primary tenorrhaphy * Provided signed informed consent * Agreed to attend follow-up visits and comply with the study protocol Exclusion Criteria: * More than one extensor tendon laceration in the same hand * Injuries involving the thumb * Tendon injuries with loss of substance * Associated injuries at the same level (e.g., bone fracture, nerve lesion) * Patients with cognitive impairment or inability to follow the protocol * Presence of other injuries or medical conditions that could interfere with assessment

What they're measuring

Change in Grip Strength of the Injured Hand

Timeframe: 4 and 6 weeks after injury

Trial details

NCT IDNCT06950268

SponsorFundacin Biomedica Galicia Sur

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-08-25

View on ClinicalTrials.gov More Hand Injuries trials