The effect of intravenous paracetamol and ketorolac for prevention of intraoperative shoulder pai
Phase 2
Recruiting
- Conditions
- cesarean delivery.Delivery by caesarean section, unspecifiedO82.9
- Registration Number
- IRCT20180922041084N4
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
primi-gravid or second gravid
elective cesarean section (ASA I-II) who have singleton pregnancy at term (37 weeks of gestational age or more
singleton pregnancy
37 weeks of gestational age or more
Exclusion Criteria
allergy to ketorolac and other NSAIDs
allergy to paracetamol
asthma
gestational diabetes
cardiovascular disorders
hepatic disorders
renal insufficiency
chronic alcoholism
per-eclampsia
bleeding tendency
chronic pain
history of upper extremity trauma
history of peptic ulcer disease
history of abdominal surgery
any contraindication to spinal anesthesia
spinal column fracture
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Shoulder pain. Timepoint: Before the surgery as baseline measurement and intra-operatively. Method of measurement: numerical rating scale (NRS).;Blood pressure. Timepoint: Every five minutes till 20 minutes after spinal anesthesia and the every 10 minutes to the end of the surgery. Method of measurement: Monitoring.;Heart rate. Timepoint: Every five minutes till 20 minutes after spinal anesthesia and the every 10 minutes to the end of the surgery. Method of measurement: Monitoring.
- Secondary Outcome Measures
Name Time Method Hematocrit. Timepoint: Before and after surgery. Method of measurement: Blood sample.