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Comparision of precautionary dose of intravenous bolus versus infusion dose of phnylephrine for prevention of spinal anaesthesia induced hypotension in elective cesarean section

Comparison of prophylactic intravenous bolus versus infusion of phenylephrine for preventing spinal anesthesia-induced hypotension in elective cesarean sections - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079107
Enrollment
70
Registered
2025-01-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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: Spinal Anaesthesia: The Spinal Anaesthesia will be given after confirming free flow of CSF 0.5% heavy bupivacaine 2.4ml will be given . Control Intervention1: phenylephrine: Group A: Co

Sponsors

SGRD
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All the patients who are undergoing cesarean section or the patients falling under American Society of Anesthesiology (ASA) Grade II

Exclusion criteria

Exclusion criteria: 1. Contraindications to regional anesthesia such as anatomic disorders of spine, shock, local site infections, peripheral neuropathy. 2. Patients with the history of hypertension or pregnancy induced hypertension. 3.Patients with hypersensitivity to study drugs . 4.Patients with coagulation disorders and bleeding disorders. 5.Patients with cardiovascular or cerebrovascular disorders 6. Patients with fetal abnormality

Design outcomes

Primary

MeasureTime frame
to assess the effect of prophylactic doses of intravenous bolus versus infusion of phenylephrine for prevention of spinal induced hypotension in elective cesarean section. Timepoint: Continuous intraoperative, vitals will be recorded every 2min interval for first 10min and then at 5 min interval till the end of surgery. outcome will also be assessed in post anaesthetic care unit (PACU) at 15min interval.

Secondary

MeasureTime frame
To assess intaoperative complications related to study drug. To calculate apgar scoreat 1 and 5 minute respectively.Timepoint: Throughout during the surgery and APGAR score will be assessed immidiatly and after 5 minutes of birth

Countries

India

Contacts

Public ContactDr Sakshi

Sri Gur Ram Das Institute of Medical Sciences and Research, Mehta Road, Vallah, Amritsar

sgrdanaesthesia@gmail.com9815632909

Outcome results

None listed

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