Regional anesthesia in surgery for carpal tunnel syndrome
Not Applicable
- Conditions
- Carpal tunnel syndrome.Carpal tunnel syndrome
- Registration Number
- IRCT2014090912642N5
- Lead Sponsor
- Vice chancellor for research, Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
age more than 18; ASA I,II. Exclusion criteria: the reluctance of patients to participate in the study; peripheral vascular disease or peripheral vascular access failure; arteriovenous shunt or venous system dysfunction; severe liver failure ; sickle cell anemia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The time of complete of nerve block. Timepoint: Post intervention. Method of measurement: With control of pain and heat sensory, based on second.;Patient pain score. Timepoint: Before, during and immediately after operation. Method of measurement: With use of VAS score.;The time of need for analgesic drug. Timepoint: After end of surgery and with interval of one hour. Method of measurement: According to the first time prescribing analgesic drug, based on second.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: Before, during and immediately after surgery. Method of measurement: With Analog pressure gauge.;Heart rate. Timepoint: Before, during and immediately after surgery. Method of measurement: With pulseoxymetery device and based on beat on minute.;Arterial oxygen saturation. Timepoint: Before, during and immediately after surgery. Method of measurement: With pulseoxymetery device and based on percentage.