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Comparison of two different volumes of intravenous fluid administration after spinal anaesthesia for prevention of hypotension in elective caesarean section.

COMPARISION OF TWO DIFFERENT VOLUMES OF CRYSTALLOID CO- LOADING ON PREVENTION OF SPINAL ANAESTHESIA INDUCED HYPOTENSION DURING CAESAREAN DELIVERY; A RANDOMISED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/031380
Enrollment
86
Registered
2021-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical Health 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

Interventions

Intervention1: Nil: Nil Intervention2: Intravenous fluid- Ringers lactate: Ringers lactate fluid administration to prevent spinal anaesthesia induced hypotension Control Intervention1: Nil: Nil Contro

Sponsors

Vijayanagar Institute Of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
To study the effect of varying volumes of crystalloid co-loading in preventing hypotension in caesarean section under spinal anaesthesia. Timepoint: After spinal anaesthesia.—

Secondary

MeasureTime frame
To assess the requirement of vasopressors, other haemodynamic changes, neonatal outcomes and others.Timepoint: After spinal anaesthesia—

Countries

India

Contacts

Public ContactDrBala Bhaskar S

Vijayanagar Institute Of Medical Sciences,Ballari

ashpatil25101994@gmail.com9108238514

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026