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Requirement of phenylephrine to treat fall in blood pressure after spinal anaesthesia in two different types of preeclampsia patients

Comparison of phenylephrine requirements to treat post-spinal hypotension in early onset and late onset preeclampsia patients undergoing caesarean section – An analytical experimental study - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066787
Enrollment
74
Registered
2024-05-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: O149- Unspecified pre-eclampsia

Interventions

Intervention1: Early onset preeclampsia: Phenylephrine bolus administration for treatment of hypotension in patients with early onset preeclampsia undergoing caesarean section under spinal anaesthesi

Sponsors

University College of Medical Sciences and Guru Teg Bahadur Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Preeclamptic females with singleton pregnancy of 34 weeks gestation or more undergoing caesarean section under spinal anaesthesia

Exclusion criteria

Exclusion criteria: 1. Maternal complications other than preeclampsia such as chronic hypertension, other cardiovascular disease, cerebrovascular disease 2. Multiple gestation 3. Eclampsia 4. Known fetal abnormality 5. Patients with absolute or relative contra-indications for spinal anaesthesia 6. Severe fetal distress or other conditions requiring immediate induction of general anaesthesia

Design outcomes

Primary

MeasureTime frame
Total phenylephrine requirementsTimepoint: From the time of administration of spinal anaesthesia to the time of delivery of baby

Secondary

MeasureTime frame
1. Maternal haemodynamic variables 2. Total number of hypotensive episodes 3. Incidence of reactive hypertension & bradycardia 4. Neonatal Apgar scores & fetal acid-base status 5. Maternal complications such as nausea, vomiting, dizziness or any other complicationsTimepoint: From the time of administration of spinal anaesthesia to the time of delivery of baby

Countries

India

Contacts

Public ContactDr Devika S Prakash

University College of Medical Sciences and Guru Teg Bahadur Hospital

medhamohta@gmail.com9625900626

Outcome results

None listed

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