Treatment of Proximal Interphalangeal Joint Injuries. Clinical Efficiency of Syndactyly Treatment and Digital Compression

Vaud University Hospital Center

Status: Terminated

Conditions: Finger Injuries

Treatments: Device: Rigid splint without compression; Device: Rigid splint with compression; Device: Syndactyly with compression; Device: Syndactyly without compression

Study type: Interventional

Funder types: Other

Identifiers

NCT02548260

301/15

Details and patient eligibility

About

Proximal interphalangeal joint injuries of the fingers may be treated in various ways and no treatment has been shown to be superior. The investigators wish to study the effectiveness of syndactyly versus digital splint when comparing joint mobility. The investigators also wish to study the effectiveness of finger compression in reducing edema and therefore allowing a greater arc of motion.

Full description

Proximal interphalangeal joint (PIPJ) injuries of the fingers are a common occurrence. They may be treated various ways: strict immobilization in a finger splint for one to three weeks, syndactyly, no immobilization. Immobilization is often responsible for joint stiffness whereas immediate mobilization might produce pain.

Injuries to the joints of the hand produce edema that is responsible for additional stiffness. Compressive garment may be worn to limit the extent of the edema and help its resorption.

Although PIPJ injuries are frequent, their treatment does not benefit from a consensus. Most studies are retrospective or aimed at a pediatric population. The investigators wish to evaluate the outcome of PIPJ injury after different treatments: either strict immobilization in a rigid splint for three weeks, of relative immobilization in a syndactyly for three weeks.The investigators also wish to study the effect of finger compression on edema resolution and finger motion. Therefore there will be four treatment groups: syndactyly with and without compression, rigid splint with and without compression.

The study will be conducted in the hand surgery unit of a university hospital in a prospective way. The assignment to a particular treatment group will be randomly performed. Patients will be followed for 6 months.

Enrollment: 33 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• proximal interphalangeal joint injury with or without dorsal or lateral luxation
• less than seven days after injury
• injured joint stability
• fracture of the palmar rim of the intermediate phalanx less than 30% of articular surface

Exclusion criteria

• palmar luxation of the proximal interphalangeal joint
• fracture of the palmar rim of the intermediate phalanx greater than 30% of articular surface
• injury to the central band of the extensor tendon
• fracture other than palmar rim of the intermediate phalanx less than 30% of articular surface
• non reducible luxation

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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33 participants in 4 patient groups

Syndactyly without compression

Experimental group

Description:

Relative immobilization with a syndactyly (CE conformity), no compression is worn.

Treatment:

Device: Syndactyly without compression

Syndactyly with compression

Experimental group

Description:

Relative immobilization with a syndactyly (CE conformity), compression (CE conformity) is worn over the finger

Treatment:

Device: Syndactyly with compression

Rigid splint without compression

Experimental group

Description:

Rigid immobilization with a custom made thermoplastic splint (CE conformity), no compression is worn

Treatment:

Device: Rigid splint without compression

Rigid splint with compression

Experimental group

Description:

Rigid immobilization with a custom made thermoplastic splint (CE conformity), compression (CE conformity) is worn over the finger

Treatment:

Device: Rigid splint with compression