Evaluating the quality of Intra-Venous Regional Anesthesia (IVRA) following adding Dexamethasone or TNG to Lidocaine
Not Applicable
- Conditions
- Intravenous Regional Anesthesia.
- Registration Number
- IRCT2015053122511N1
- Lead Sponsor
- rmia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
male or female patients; scheduled for hand or forearm surgery with I & II physical status of ASA; aged between 20 and 50 years.
Exclusion criteria: Patients with sickle cell anemia; Raynaud's disease; history of drug allergy.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The onset time of sensory block. Timepoint: every 30 sec. Method of measurement: Pinprick test.;The onset time of motor block. Timepoint: every minute. Method of measurement: ability to flex and exten wriet and fingures.;The onset time of tourniquet pain. Timepoint: in 1, 5, 10, 20, and 30 minutes. Method of measurement: visual analog scale of pain.;The recovery time from sensory block. Timepoint: every 30 sec. Method of measurement: Pinprick test.;The recovery time from motor block. Timepoint: in 1, 5, 10, 20, and 30 minutes. Method of measurement: ability to flex and exten wriet and fingures.
- Secondary Outcome Measures
Name Time Method The amount of analgesic consumptions. Timepoint: If patient reported VAS>3. Method of measurement: 1 micro gr/kg.