Effect of naloxone on ileus after caesarean section by spinal anesthesia
Phase 2
Completed
- Conditions
- ileus.Ileus, unspecified
- Registration Number
- IRCT2016022426357N2
- Lead Sponsor
- Mazandaran University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Inclusion criteria (inclusion criteria): The willingness of patients to participate in the study and informed consent; first elective cesarean section under spinal anesthesia; Age> 18 years; ASA Class ? Exclusion criteria (exclusion criteria): Any contraindication to spinal anesthesia; Taking prokinatic; Irritable Bowel Syndrome; drug addiction;
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Ileus. Timepoint: as soo. Method of measurement: Upon arrival to the recovery room, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 6, 12 and 24 hours after operation.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: Upon arrival to the recovery room, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 6, 12 and 24 hours. Method of measurement: VAS.;VOMITING. Timepoint: Upon arrival to the recovery room, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 6, 12 and 24 hours. Method of measurement: VAS.;NAUSEA. Timepoint: Upon arrival to the recovery room, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 6, 12 and 24 hours. Method of measurement: VAS.;Itching. Timepoint: Upon arrival to the recovery room, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 6, 12 and 24 hours after surgery. Method of measurement: VAS.