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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00981565
Other study ID # NKCH-Surg-005
Secondary ID
Status Completed
Phase N/A
First received September 11, 2009
Last updated October 17, 2012
Start date September 2009
Est. completion date June 2012

Study information

Verified date October 2012
Source North Karelia Central Hospital
Contact n/a
Is FDA regulated No
Health authority Finland: North Karelia Central Hospital, clinic of surgery
Study type Interventional

Clinical Trial Summary

Carpal tunnel syndrome (CTS) is the most common peripheral nerve entrapment. Diagnosis is based on symptoms, clinical findings and electrophysiological examination. Several conservative and surgical treatment options have been described.

Studies of surgical versus conservative treatment in mild carpal tunnel syndrome have not been done and it is still unclear whether or not surgical treatment is better than conservative treatment.

The aim of this study is to research has surgery better outcome in mild CTS than conservative treatment. Patient satisfactory, clinical and electrophysiologic outcomes, direct and indirect costs will be evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date June 2012
Est. primary completion date September 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- electrophysiologically proven minimal or mild CTS lasting more than six months will be included in this study

Exclusion Criteria:

- rheumatoid arthritis

- diabetes mellitus

- hypothyreosis

- pregnancy

- wrist trauma or previous surgery

- splinting or corticosteroid injection on the affected side

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
open carpal tunnel release
surgery to release the carpal tunnel
Other:
Night-cast
individual night time splinting

Locations

Country Name City State
Finland North-Carelia Central Hospital Joensuu
Finland Kuopio University Hospital Kuopio
Finland Central Hospital of Mikkeli Mikkeli

Sponsors (1)

Lead Sponsor Collaborator
North Karelia Central Hospital

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Symptom Severity Score 1 year No
Primary Pain Visual Analogue Scale (VAS) 1 year No
Secondary Change in electroneuromyography 1 year No
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