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Comparing two doses of intravenous ondansetron in LSCS patients on spinal anaesthesia

Efficacy of two doses of Intravenous Ondansetron on spinal anaesthesia induced hypotension and bradycardia in patients undergoing LSCS: A Comparative study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097710
Enrollment
90
Registered
2025-11-19
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

None listed

Interventions

Intervention1: Spinal Anaesthesia: Patient in sitting position by using 25G Spinal needle Lumber puncture done at L3-L4 or L4-L5, free flow of CSF noted. 2 ml of 0.5% hyperbaric bupivacaine given to i

Sponsors

Sapthagiri Institute of Medical Sciences and Research Centre Department of Anaesthesia
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Parturients scheduled for elective cesarean section under spinal anaesthesia 2 Aged 18 to 40 years 3 ASA physical statusII 4 Written informed consent

Exclusion criteria

Exclusion criteria: 1 Allergy to study drugs 2 Pregnancy-induced hypertension (PIH) 3 Presence of any other comorbid conditions

Design outcomes

Primary

MeasureTime frame
Incidence of hypotension SBP less than 90mmhg or morethan 20 percent decrease from baseline and bradycardia HR less than 60bpmTimepoint: Incidence of hypotension SBP less than 90mmhg or morethan 20 percent decrease from baseline and bradycardia HR less than 60bpm—

Secondary

MeasureTime frame
Vasopressor requirement and incidence of shiveringTimepoint: From induction of spinal anaesthesia to 120 minutes—

Countries

India

Contacts

Public ContactDR PRABHA P

Sapthagiri Institute of Medical Sciences and Research Centre

prabhap1510@gmail.com9448055973

Outcome results

None listed

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