RecruitingACTRN12625000758404

A randomised comparative trial of patients following surgical repair of finger flexor tendons, comparing the effect of two splints, on patient-reported hand function and quality of life and clinician-reported range of motion and grip strength.

A randomised comparative trial of patients following surgical repair of finger flexor tendons, comparing the effect of a Manchester short splint versus a forearm-based dorsal blocking splint, on patient-reported hand function and quality of life and clinician-reported range of motion and grip strength.


Sponsor

Nicola Williams, Royal Adelaide Hospital

Enrollment

66 participants

Start Date

Oct 27, 2025

Study Type

Interventional

Conditions

Summary

The aim of this study is to compare outcomes between two splints used after surgical repair of flexor tendon injury, namely the forearm-based dorsal blocking splint and Manchester short splint. Outcomes will include patient-reported hand function and quality of life, and clinician-reported range of motion and grip strength.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

Cutting a finger flexor tendon — the tendon that allows you to bend your fingers — is a serious injury that requires surgery and careful rehabilitation. After the repair, the hand is usually placed in a protective splint while healing occurs. Two splints are currently used: the traditional forearm-based dorsal blocking splint (which is longer and more restrictive) and the shorter Manchester short splint (which allows more wrist movement). It is not yet clear which one leads to better outcomes. This randomised trial will compare the two splints directly, measuring hand function, quality of life, range of motion, and grip strength at multiple points during the recovery process. Participants will be randomly assigned to one splint type after their surgery. This study is open to adults admitted to the Royal Adelaide Hospital with a traumatic finger flexor tendon injury who undergo surgical repair. People with major associated injuries (such as fractures or significant nerve damage), those unable to commit to follow-up appointments, or those on WorkCover are not eligible.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

The study intervention is the Manchester short splint. This is a splint that extends from the back of the wrist crease to the fingertips. As per usual clinical practice, this splint will be custom-mad

The study intervention is the Manchester short splint. This is a splint that extends from the back of the wrist crease to the fingertips. As per usual clinical practice, this splint will be custom-made by a hand therapist (physiotherapist or occupational therapist) and applied within the first 5 days post-operatively, with instructions to wear the splint full time for the first 6 weeks post-operatively (this may be shortened to approximately 5 weeks if indicated due to severe adhesions/stiffness and/or difficulty regaining range of motion, as per usual clinical practice). The position of joints within the splint will, as per usual clinical practice, be customised for the zone of repair and the position modified if required by individual factors such as associated nerve repair/tension. Participant feedback about adherence to splint wear will be recorded.


Locations(1)

The Royal Adelaide Hospital - Adelaide

SA, Australia

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ACTRN12625000758404