painless effect of the injected tramadol in the Cesarean Section incisio
Not Applicable
- Conditions
- Postoperative Pain.Pain localized to other parts of lower abdomen
- Registration Number
- IRCT2013070111662N2
- Lead Sponsor
- Vice-Chancellery of Research and Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 49
Inclusion Criteria
About 98 females who will candidate for elective cesarean section under general anesthesia wil bel enrolled in this study.
Exclusion criteria: Emergency surgery; Cardiopulmonary disorders; Allergic reaction to drugs use in study; Alcohol addiction; Addiction to opium or other illicit drugs; Chronic pain syndrome; Convulsion.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain intensity. Timepoint: Every one hour in the first postoperative 24 hr. Method of measurement: Visual Anlouge Scale.
- Secondary Outcome Measures
Name Time Method Respiratory depression. Timepoint: Every one hour during first postoperative 24 hr. Method of measurement: Respiratory depression is defined as respiratory rate less than 8 per min.;Nausea and Vomiting. Timepoint: Every one hour during first postoperative 24 hr. Method of measurement: Nausea is defined as urge to vomiting without ejection ofof the contents of the stomach through the mouth, Vomiting is defined asto eject of the contents of the stomach through the mouth, usually in a series of involuntary spasmic movements.