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Temperature measurement in the emergency cesarean section undergoing mothers under spinal anaesthesia

Temperature monitoring with Zeroflux Probe in Parturient undergoing Emergency Cesarean Section under Spinal Anaesthesia – An Observational Study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/09/073654
Enrollment
230
Registered
2024-09-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Intervention1: Nil since its an observational study: Nil since its an observational study Control Intervention1: Nil since its an observational study: Nil since its an observational study

Sponsors

Jawaharlal institute of postgraduate medical education and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Emergency cesarean section under spinal anaesthesia

Exclusion criteria

Exclusion criteria: 1. Patients planned for the section under GA 2. Failed or inadequate neuraxial technique, converted to GA 3. Patients with preexisting fever or sepsis.

Design outcomes

Primary

MeasureTime frame
To observe the incidence of hypothermia in patients undergoing emergency cesarean section under spinal anesthesiaTimepoint: 5 minutes after they shifted to PACU—

Secondary

MeasureTime frame
a)To determine the association of maternal hypothermia with the following, 1.Baseline maternal temperature 2.Maternal temperature during delivery 3.Duration of surgery 4.Amount of IV fluids administered b)To measure the usage of warm IV fluids (37-41ºC),warming blankets and forced air warmers in emergency cesarean section. Timepoint: During surgery and in PACU—

Countries

India

Contacts

Public ContactDr Sivakaran R

Jawaharlal institute of postgraduate medical education and research

priyaab8@gmail.com8903468132

Outcome results

None listed

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