the analgesic effect of lidocaine-ketorolac and lidocaine in upper limb surgery
Phase 2
Completed
- Conditions
- regional anesthesia.Local anaesthetics
- Registration Number
- IRCT2015082420020N2
- Lead Sponsor
- Vice chancellor for research,babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
15 to 70-year-old patients with upper extremity surgery with ASA class 1,2 are enrolled.
Exclusion criteria: patients with lidocaine allergy, emergency patients, addict and psychological disorders.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative Pain. Timepoint: 1, 6, 12, 24 Hours after operation. Method of measurement: VAS scale pain.;Overall analgesic requirement post operative. Timepoint: in the first 24 hours after operation. Method of measurement: Nursing Report.;Onset sensory block. Timepoint: From the start of anesthetics injection. Method of measurement: Evaluate the patients response to needle hitting on surgical site.;Tourniquet site pain. Timepoint: Tourniquet pain expressed by patients after applying the tourniquet and during surgery. Method of measurement: Visual Analogue Scale (VAS).
- Secondary Outcome Measures
Name Time Method