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The carpal tunnel syndrome. Clinical definite CTS with normal electrodiagnostic studies and diagnostic value sonography.

The carpal tunnel syndrome. Clinical definite CTS with normal electrodiagnostic studies and diagnostic value sonography. - The carpal tunnel syndrome.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29793
Enrollment
160
Registered
2006-08-11
Start date
2006-05-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

tunnelsyndrome

Interventions

A: Patients in group 1 will be treated surgically with open release of the carpal tunnel. The operation is carried out by a neurosurgeon. Patients in group 2 are treated conservatively. B: There is

Sponsors

Canisius Wilhelmina Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Paresthesia or pain in de area supplied by median nerve, with at least 2 of the following: nocturnal complaints, improvement by Flick's sign, worsening with handmovements. Normal electrodiagnostic investigation of the median nerve.

Exclusion criteria

Exclusion criteria: Clinical polyneuropathy, Trauma, bad general condition with reduced life expectancy, severe atrophy of m. Abductor pollicis brevis, pregnancy, alcoholism, arthritis of arthrosis, known diabetes mellitus, reumatoid arthritis, thyroid pathology, HNLPP, languagebarrier, psychiatric problem, other neurological problems in arm, former surgery, refusal surgery, age younger than 18, participance in other trials

Design outcomes

Primary

MeasureTime frame
A: Primairy outcome measure: the percentage of patients with no complaints after 6 months. B: Primairy outcome measure: the percentage of patients with clinical definite and probable CTS with ultrasonography meeting the criteria of CTS.

Secondary

MeasureTime frame
A: Secundairy outcome measures: 1. The percentage of patients with an improvement of the Functional Status Score with 40 % or more after 6 months. 2. The percentage of patients in group 2 who are operated on after 6 months. 3. The percentage of patients in group 1 with persistent complaints of CTS. 4. The percentage of patients with ultrasonography meeting the criteria of CTS. B: Secundairy outcome measure: The correlation between nerve conduction studies and ultrasonography in patients with clinical definite and probable CTS.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)