Comparison of the effect of dexmedetomidine and lower dose of neostigmine in pain relief after cesarean section with spinal anesthesia
Phase 3
Recruiting
- Conditions
- Severity of pain.Pain, unspecified
- Registration Number
- IRCT20210904052371N4
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 102
Inclusion Criteria
Women who had an elective cesarean delivery
Women who are between 18 and 50 years old.
Exclusion Criteria
Patients who refused to participate, or after spinal anesthesia, the required sensory level was not established and were then subjected to general anesthesia.
Patients with a history of allergy to any of the drugs used in this research
History of drug addiction
Moderate or severe heart, kidney, lung or nervous diseases
Significant scoliosis or kyphosis
Excessive obesity
Blood coagulation disease
Patients with height less than 130 cm or BMI more than 35
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of pain. Timepoint: 0, 2, 4, 8 and 12 hours. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Sedation rate. Timepoint: Hours 0, 2, 4, 8 and 12. Method of measurement: Using the Ramsay scale.