Comparison of two oral precursors of melatonin and gabapentin in female candidates for cesarean section under spinal anesthesia
Phase 2
Recruiting
- Conditions
- Evaluation of pain and anxiety in female candidates for cesarean section under spinal anesthesia.
- Registration Number
- IRCT20190120042432N1
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 93
Inclusion Criteria
full-term pregnant women aged 18 to 40 years old undergoing elective cesarean section under spinal anesthesia
Exclusion Criteria
contraindications for gabapentin or melatonin
failed or partial spinal anesthesia
gravidity more than 3
Intrauterine Growth Restriction
fetal distress
history of alcoholism, drug abuse ,convulsion, migraine, dicopathy ,hepatitis ,renal failure ,cardiovascular or pulmonary diseases ,preeclampsia or eclampsia, hypertension, diabete
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The rate of anxiety and postoperative pain. Timepoint: Based on the Verbal Anxiety Scale, anxiety and pain levels is measure before premedication, before spinal anesthesia, five minutes after spinal anesthesia, after exiting the infant, and 15 minutes after spinal anesthesia as well as after surgery and patient transmission to recovery. Method of measurement: With using the Verbal Anxiety Scale.
- Secondary Outcome Measures
Name Time Method The amount of the analgesic drug. Timepoint: Within 12 hours after surgery. Method of measurement: 5 cc syringe using for drug injection.