compairing the effects of neuroaxial and general anesthesia on postoperative quality of recovery after abdominal hysterectomy.
Phase 2
- Conditions
- Post operative analgesia after total abdominal hysterectomy.Acquired absence of uterusZ90.710
- Registration Number
- IRCT201309306148N3
- Lead Sponsor
- Vice-chancellor Of Research Babol University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
ASA physical status I and II females undergoing total abdominal hysterectomy for benign (noncancerous) disease.
Exclusion criteria: Patients with a history of coagulopathy; recent infectioncurrent; use of an opioid analgesic or corticosteroid; history of migraine headache; gross neurologic impairment; suspected difficult airway
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Analgesia. Timepoint: 6, 24, 48 hour after surgery. Method of measurement: Visual analogues Scale.;Quality of recovery. Timepoint: 24, 48 hour after surgery. Method of measurement: QOR-40 questionnaire.
- Secondary Outcome Measures
Name Time Method Heart Rate. Timepoint: Before induction, during surgery and after surgery. Method of measurement: ECG.;Blood Pressure. Timepoint: Before induction of anesthesia, during surgery and after surgery. Method of measurement: Non invasive BP Cuff.;Nausea & Vomiting. Timepoint: After Surgery. Method of measurement: Question & Observation.