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Surgical Versus Conservative Treatment of Acute Mallet Fingers; a Randomised Controlled Trial

Surgical Versus Conservative Treatment of Acute Mallet Fingers; a Randomised Controlled Trial

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01016197
Enrollment
0
Registered
2009-11-19
Start date
2010-01-31
Completion date
2011-06-30
Last updated
2016-09-27

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

Conditions

Finger Injury

Keywords

Soft tissue mallet finger

Brief summary

The investigators are investigating if surgical treatment of injuries to the tendon which straightens the finger tip gives a better functional outcome than treatment with a splint while the tendon heals.

Detailed description

The investigators will randomise patients to receive splinting of their finger while their tendon heals or have surgical intervention. Surgical intervention will entail fixing the tendon with bone anchors and splinting. Conservative treament involves splinting while the tendon heals. We will then monitor the functional outcome of the hand using the DASH questionare over 18 months.

Interventions

PROCEDUREextensor tendon repair

Surgical repair of extensor tendon with bone anchor and splinting

PROCEDUREMallet splint for 4 weeks

The patient will wear a mallet splint for fours weeks and then mobilise their finger.

Sponsors

Mid Cheshire Hospitals NHS Foundation Trust
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* soft tissue mallet finger * acute injury

Exclusion criteria

* ASA 3 or above * Unable to give informed consent * Infection in digit affected

Design outcomes

Primary

MeasureTime frame
DASH scoreup to 18 months

Secondary

MeasureTime frame
Range of movement at distal interphalyngeal joint.3, 6, 12 and 18 months

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026