Treatment for Cubital Tunnel Syndrome

NCT ID: NCT00184158

Last Updated: 2017-08-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

81 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-01-31

Study Completion Date

2009-01-31

Brief Summary

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The researchers want to find out the best treatment for cubital tunnel. The researchers establish the degree of nerve compression and then the patients are randomised to different treatment alternatives, ranging from conservative to operative treatments.

The study is performed at 5 different hospitals in Norway.

Detailed Description

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Conditions

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Cubital Tunnel Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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decompression

Conservative, simple decompression and nerve transfer

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients with cubital tunnel syndrome

Exclusion Criteria

* Rheumatoid arthritis (RA)
* Osteoarthrosis
* Varus or valgus deformities at elbow
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Norwegian University of Science and Technology

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Vilhjalmur Finsen, Prof

Role: STUDY_DIRECTOR

National Taiwan Normal University

Locations

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St Olavs Hospital

Trondheim, , Norway

Site Status

Countries

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Norway

Other Identifiers

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056-02

Identifier Type: -

Identifier Source: org_study_id

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