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Effect of endoscopic surgery in comparison with open method in carpal tunnel syndrome

Clinical Trial study for comparison of endoscopic carpal tunnel release in patients with median nerve compressive neuropathy with open method

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013040612914N1
Enrollment
176
Registered
2013-05-18
Start date
2007-01-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Patients with Carpal Tunnl Syndrome (with positive signs in physical exam and also electro-myography). Carpal Tunnel Syndrome

Interventions

Intervention 1: Intervention for treatment group is one-portal endoscopic method for carpal tunnel release with Microaire instrument per standard technique will be implemented. According to the type o
Treatment - Surgery
Intervention for treatment group is one-portal endoscopic method for carpal tunnel release with Microaire instrument per standard technique will be implemented. According to the type of intervention (
For control group the open surgery method will be applied.

Sponsors

Sciences Vice chancellor for research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
41 Years to 64 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: all patients with the history of recurrent or persistent parethesia in the median nerve territory, worsening of symptoms with hand activity, nocturnal paresthesia and presence of positive Tinnel's and/or Phalen's signs on physical examination and also positive electro-myography; Exclusion criteria: previous carpal tunnel surgery, incomplete records, trauma, patients' refusal to participate in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 0ne, three, six months and one year after operation. Method of measurement: Thermometer visual tool.;Paresthesia. Timepoint: 0ne, three, six months and one year after operation. Method of measurement: Standard check list.

Secondary

MeasureTime frame
Grip strength measurement. Timepoint: One, three and six months and one year after operation. Method of measurement: Jamar dynamometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahram Nazerani

Iran University of Medical Sciences

snazerani@yahoo.com+98 21 2254 1429

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026