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NCT00184158 Clinical Trial

Treatment for Cubital Tunnel Syndrome

Cubital Tunnel Syndrome Clinical Trial

Official title:
Cubital Tunnel Treatment, Evaluation of Conservative and Operative Alternatives

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00184158
Other study ID # 056-02
Secondary ID
Status Completed
Phase N/A
First received September 12, 2005
Last updated August 17, 2017
Start date January 2005
Est. completion date January 2009

Study information
Verified date August 2017
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 81
Est. completion date January 2009
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients with cubital tunnel syndrome

Exclusion Criteria:

- Rheumatoid arthritis (RA)

- Osteoarthrosis

- Varus or valgus deformities at elbow

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• decompression
Conservative, simple decompression and nerve transfer

Locations
Country Name City State
Norway St Olavs Hospital Trondheim

Sponsors (1)
Lead Sponsor Collaborator
Norwegian University of Science and Technology

Country where clinical trial is conducted

Norway, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain
Secondary electroneurography (ENG electroneurography (ENG) before and after the operation and to see if it is consistent with the patient evaluation.
Secondary paresthesia
Secondary weakness
Secondary patient satisfaction
See also
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