Effects of intrathecal midazolam on block characteristic and control of postoperative pai
Phase 4
- Conditions
- Regional anesthesia.Local anesthetics
- Registration Number
- IRCT2016063028712N1
- Lead Sponsor
- Vice chancellor for research of Kurdistan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
1) take Informed consent to enter the study; 2) patients between 20-70 old age; 3) Physical status 1 and 2 classification of American Society of Anesthesiologists(ASA).
Exclusion criteria: 1) Ischemic heart disease; 2) Hypertension; 3) Uncontrolled diabetes; 4) Valvular heart disease; 5) Coagulopathy; 6) Lumbar spinal column deformity; 7) Block failure due to technical problems; 8) Needs to extra sedative drugs.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of sensory block. Timepoint: During first ten minute after block. Method of measurement: Cold cotton.;Intensity of motor block. Timepoint: During first ten minute after block. Method of measurement: Bromage scale.;Duration of sensory block. Timepoint: The time to regresion of sensory block to S1 in PACU. Method of measurement: Cold cotton.;Duration of motor block. Timepoint: The time to regression of motor block to bromage 1 in PACU. Method of measurement: Bromage scale.
- Secondary Outcome Measures
Name Time Method Pain scale. Timepoint: In discharge time and three houre later. Method of measurement: Numerical rating scale.;Nausea and vomiting. Timepoint: Time of block until discharge from recovery(PACU). Method of measurement: Questionnaire.;Shivering. Timepoint: Time of block until discharge from recovery(PACU). Method of measurement: Observation of face and extermitis.;Hypotension. Timepoint: First 15 minute after block every 2 minute and then every 15 minute. Method of measurement: Monitoring.;Bradycardia. Timepoint: First 15 minute after block every 2 minute and then every 15 minute. Method of measurement: Monitoring.;The time to first analgesic request. Timepoint: 3 houre after discharge of recovery. Method of measurement: File.