Comparison of two different volumes of intravenous fluid administration after spinal anaesthesia for prevention of hypotension in elective caesarean section.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: Y838- Other surgical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure
- Registration Number
- CTRI/2021/02/031380
- Lead Sponsor
- Vijayanagar Institute Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Primiparous and multiparous parturient women with 37â??42 weeks of gestation
1.Singleton pregnancy
Posted for elective caesarean section under spinal anaesthesia.
2.ASA grade II
3.Normal foetal profile
4.Patients only on maintenance flow of IV fluids
Exclusion Criteria
1.Contraindication for or refusal of spinal anaesthesia
2.Hypertension (SBP >140 mm Hg or DBP >90 mm Hg) due to Chronic or gestational hypertension or preeclampsia
3.Cardiovascular and/or cerebrovascular diseases
4.Diabetes mellitus
5.Hypersensitivity to fentanyl or bupivacaine
6.Obesity
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study the effect of varying volumes of crystalloid co-loading in preventing hypotension in caesarean section under spinal anaesthesia. <br/ ><br>Timepoint: After spinal anaesthesia. <br/ ><br>
- Secondary Outcome Measures
Name Time Method To assess the requirement of vasopressors, other haemodynamic changes, neonatal outcomes and others.Timepoint: After spinal anaesthesia