Analgesic Effect of Adding Midazolam and Fentanyl to Intrathecal Bupivacaine 0.05%
Not Applicable
- Conditions
- Pain.Pain in limb
- Registration Number
- IRCT2014061810340N9
- Lead Sponsor
- Golestan University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
people aged 18-65 years that categorized into class 1 and 2 based on America Society of Anesthesiologists (ASA); Exclusion criteria : rejection of patients with substance abuse, patients with symptoms of neuropathy, and lack of appropriate sensory level after performing the spinal anesthesia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analgesia. Timepoint: After intervention. Method of measurement: Duration of analgesia.
- Secondary Outcome Measures
Name Time Method Hemodynamic Change. Timepoint: Before Intervention, 30 ,60 and 90 minutes after intervention. Method of measurement: Sphygmomanometer, Pols oximeter.;Chills. Timepoint: After intervention. Method of measurement: Observation.;Nausea. Timepoint: After intervention. Method of measurement: Observation.;Vomiting. Timepoint: After intervention. Method of measurement: Observation.