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oxygen perfusion from saturation probe as a index of hypotension following spinal anesthesia in elective caesarean surgery

perfusion index derived from pulse oximeter as a predictor of hypotension following spinal anaesthesia in elective caesarean delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/03/050192
Enrollment
100
Registered
2023-03-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

None listed

Sponsors

DR NETHRA S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I and II BMI gestational age between 36 â?? 40 weeks

Exclusion criteria

Exclusion criteria: Unwilling to participate in the study Contraindications to regional anesthesia Those requiring emergency caesarean section Pregnancy induced hypertension or preeclampsia Gestational diabetes mellitus Twin gestation, placenta previa BMI >= 40, blood loss > 1000 ml Failure to achieve sensory block to T6 dermatome Gestational age 40 weeks Cardiovascular or cerebrovascular disease

Design outcomes

Primary

MeasureTime frame
To determine whether baseline perfusion index can be used to predict hypotension following spinal anesthesia for the elective lower segment caesarean delivery. Timepoint: within a minute after attaching pulse oximeter(baseline)—

Secondary

MeasureTime frame
nilTimepoint: nil—

Countries

India

Contacts

Public ContactARUN KUMAR H D

KMC MANIPAL

arunhd2000@yahoo.com9008415858

Outcome results

None listed

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