The effect of fentanyl and dexmedetomidine as adjuvants on pain after cesarean sectio
Phase 3
Recruiting
- Conditions
- Evaluation of pain in patients after cesarean section with spinal anesthesia by marcaine and dexmedetomidine.
- Registration Number
- IRCT20211012052747N1
- Lead Sponsor
- Birjand University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
Having informed consent to enter the study
ASA Class 1 and 2
Term pregnancy
Singleton
Non-emergency cesarean section
Exclusion Criteria
Drug addiction
Dissatisfaction with spinal anesthesia
Duration of surgery more than 1 hour
Pregnancy with ASA 3 and above
Patients with head trauma
Patients with spinal deformity
Inability to position the patient
Infection in site of spinal anesthesia
Hypersensitivity to local anesthetic drugs
High ICP
Coagulation disorders and heart valve problems (especially AS)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Determine the average pain score. Timepoint: Immediately after regaining consciousness and 1, 2, 3, 4, 8 and 12 hours after surgery. Method of measurement: Using visual-auditory assessment (VAS) criteria by the study leader.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: immediately after recovery and 1, 2, 3, 4, 8 and 12 hours after surgery. Method of measurement: Sphygmomanometer.;Pulse beats. Timepoint: immediately after recovery and 1, 2, 3, 4, 8 and 12 hours after surgery. Method of measurement: Physical examination. patients' pulse is counted in one minute.