orepinephrine infusion for controlling spinal anaesthesia induced hypotension in caesarian section.
Phase 3
- Conditions
- Health Condition 1: 1- Obstetrics
- Registration Number
- CTRI/2023/08/056943
- Lead Sponsor
- Anish M
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients of age group 18 to 50 years undergoing elective caesarean section
2.Patients with ASA physical grade I or II
Exclusion Criteria
1. History of allergy to local anaesthetic agent and/ or study drugs
2. Bleeding disorders like Von Willebrand disease, ITP, platelet count <50.000/microlitre, prothrombin time > 14 seconds, International normalised ratio (INR) > 1.5
3. Local site infection
4. Spinal deformity
5. Cardiac, respiratory diseases and kidney disorder, neurological deficit
6. Parturients with PET or any hypertensive disorder.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Occurrence of hypotensionTimepoint: Outcome will be continuously recorded every 2 mins till 10 mins then every 5 mins until the end of surgery & data will be asessed at the end of 1 year
- Secondary Outcome Measures
Name Time Method Apgar score, umbilical vein blood gases record , <br/ ><br>Hemodynamic changes, norepinephrine consumption, adverse effects <br/ ><br> <br/ ><br>Timepoint: All outcomes will be continuously recorded every 2 mins till 10 mins & then every 5 mins until the end of surgery