a randomised double blinded observational study for comparison of intermittent boluses of nor-epinephrine and phenylephrine for prevention of subarachnoid block induced hypotension in cesarean sectio
Phase 3
- Conditions
- Health Condition 1: null- Pregnant Females
- Registration Number
- CTRI/2018/03/012839
- Lead Sponsor
- Dayanand Medical College Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)American society of Anesthesiologists (ASA)
physical status II undergoing lower segment
cesarean section (LSCS) under subarachnoid
block (SAB).
2)Primigravida.
3)Healthy singleton pregnancy.
4)Age more than 18 years.
5)Weight 50-100 kg.
6)Height 150-180 cm.
Exclusion Criteria
1)Onset of labour.
2)Known fetal abnormality.
3)Severe cardiovascular or cerebrovascular
disease or renal impairment.
4)Known allergy to any study medication.
5)Patients taking monoamine oxidase or
tricyclic
antidepressants.
6)Presence of mesenteric or peripheral vascular
thrombosis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method