A study to compare different infusion plans for preventing low BP and increase acid levels in foetus during elective cesarean.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/01/048781
- Lead Sponsor
- Dr K Shanmathi Devi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA physical status II patients.
2.Patient not in labour posted for caesarean section under sub arachnoid block.
3.Singleton pregnancy.
4.Gestational age of more than 36 weeks
Exclusion Criteria
1.Patients with hypertension (SBP >140mmHg, DBP > 90mmHg).
2.Diabetes mellitus.
3.Cardiovascular disease, cerebrovascular disease.
4.Known fetal anomalies.
5.Contra-indications to spinal Anaesthesia.
6.Signs of onset of labour.
7.BMI >45 kg/m2
8.Induction-delivery time of >10 minutes.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess and compare the effectiveness of different concentrations of phenylephrine infusion in preventing the maternal hypotension after the subarachnoid block for caesarean section.Timepoint: 1min,2min,3min,4min,5,min,6min,7min,8min,9min,10min,13min,16min,19min,21min,24min,27min,30min,33min,36min,39min,42min,45min
- Secondary Outcome Measures
Name Time Method To assess and compare the effectiveness of phenylephrine infusion in preventing fetal acidosis.Timepoint: 1min,2min,3min,4min,5,min,6min,7min,8min,9min,10min,13min,16min,19min,21min,24min,27min,30min,33min,36min,39min,42min,45min