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Comparison of intravenous fluid given before and during spinal anaesthesia on incidence of fall of blood pressure in cesarean delivery

Comparative study of pre-loading and co-loading with crystalloids on the incidence of hypotension after spinal anaesthesia in cesarean delivery - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070174
Enrollment
100
Registered
2024-07-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Interventions

Intervention1: 15ml/kg Ringers Lactate given before spinal anaesthesia: To record the incidence of hypotension when Ringers Lactate given before spinal anaesthesia in a Parturient undergoing elective

Sponsors

BJMedical College and Civil Hospital Ahmedabad Government of Gujarat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: parturients of ASA grade I/II posted for elective cesarean delivery giving consent for study.

Exclusion criteria

Exclusion criteria: Patient refusal, Patients with pre-existing stenotic heart disease, Known case of eclampsia, Known case of neurological disorder, History of allergy to local anaesthetics, Contraindications to spinal anaesthesia, Patients with history of bleeding disorders or on anticoagulant therapy, ASA grade IV/V

Design outcomes

Primary

MeasureTime frame
parameters compared will be SBP,DBP,MAP,PR,RR and SPO2Timepoint: parameters measured every 2min till 10min,every 5min till 30min ,every 15min till the end of surgery and then hourly till 24hours

Secondary

MeasureTime frame
Total dose of atropine required , Total dose of mephentermine required, Incidence of nausea/vomiting, APGAR SCORE Timepoint: 24hours post operative

Countries

India

Contacts

Public ContactDr Bhavana Raval

B.J. Medical College and Civil Hospital , Ahmedabad

drbhavanaraval@yahoo.com9426373182

Outcome results

None listed

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