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A Study to Access Whether Preoperative Shock Index can Predict Low Blood Pressure after Spinal Anaesthesia in women undergoing emergency cesarean delivery.

Association Between Preoperative Shock Index and Post Spinal Hypotension In Parturients Undergoing Non Elective Cesarean Section Under Spinal Anaesthesia - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/04/109411
Enrollment
115
Registered
2026-04-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil

Sponsors

Dr Nimisha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age between 18 to 40 years 2 Gestational age more than or equal to 37 weeks 3 Belonging to ASA criteria 2 4 Category 2 and 3 5 Patients undergoing non elective cesarean section under spinal anaesthesia

Exclusion criteria

Exclusion criteria: 1 Patients refusal 2 BMI more than 30kg/m2 and Height less than 150cm 3 Hypersensitivity to local anaesthetic drug 4Contraindications to spinal anaesthesia 5 Patient who is known case of antepartum haemorrhage or cardiovascular or renal diseases and Pre eclamptic patients with severe features

Design outcomes

Primary

MeasureTime frame
1To evaluate the association of preoperative Shock Index of more than 0.9 percent and post spinal hypotension in parturients undergoing non elective cesarean section under spinal anaesthesia 2 To assess the amount of intraoperative intravenous fluids and vasopressor doses used during hypotension following spinal anaesthesia Timepoint: Intra operatively—

Secondary

MeasureTime frame
To assess the following parameters following spinal anaesthesia intraoperatively and post operatively like 1 Additional requirement of uterotonics 2 Adverse effects intraoperatively and post operatively for 24 hrs Timepoint: Intraoperative and postoperative for 24 hrs—

Countries

India

Contacts

Public ContactDr Nimisha

Geetanjali Medical College and Hospital

Alkachhabra2008@gmail.com8890911487

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026