FindTrial
Sign In

A study to find ways to predict low blood pressure after spinal anesthesia in women undergoing elective caesarean delivery

A Comparative study to predict hypotension following spinal anesthesia in elective cesarean section using perfusion indexed derived from pulse oximetry and baseline hemodynamic parameters - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/12/098397
Enrollment
100
Registered
2025-12-03
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

Health Condition 1: 1- Obstetrics

Interventions

Intervention1: Nil: Nil

Sponsors

Raghuram Madireddy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant patients who are undergoing elective cesarean section of American Society of Anesthesiologist 1 & 2, with singleton live fetus more that 37 weeks of gestation

Exclusion criteria

Exclusion criteria: American Society of Anesthesiologist 3 to 6, emergency cesarean section, preterm cesarean section, allergy to local anesthetic drugs

Design outcomes

Primary

MeasureTime frame
To assess the predictive value of the perfusion index and baseline hemodynamic parameters for hypotension after spinal anesthesiaTimepoint: Baseline and then every 5 minutes for first 2 hours and then every 15 minutes for 24 hours—

Secondary

MeasureTime frame
To assess the clinical utility of perfusion index in guiding prophylactic interventionsTimepoint: 24 hours—

Countries

India

Contacts

Public ContactRaghuram Madireddy

Netaji Subhash Medical College and Hospital

faseehullah.alam@yahoo.com9155366231

Outcome results

None listed

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