Skip to content

To compare two different doses of Phenylephrine to prevent fall of blood pressure in a patient undergoing caesarean section under spinal Anaesthesia

â??Prophylactic Administration of Two Different Bolus Doses of Phenylephrine for Prevention Of Spinal â??Induced Hypotension During Cesarean Section: A prospective Double â??Blinded Clinical Studyâ??

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/12/029525
Enrollment
75
Registered
2020-12-03
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: O746- Other complications of spinal andepidural anesthesia during labor and delivery Health Condition 2: O746- Other complications of spinal andepidural anesthesia during labor and delivery

Interventions

Intervention1: Phenylephrine: Phenylephrine is a alpha 1 agonist DOSE-TWO DIFFERENT DOSAGE 75 MICROGRAM AND 100 MICROGRAM INTRAVENOUSLY IN RANDOMLY ALLOCATED PATIENTS just before spinal anaesthesia Co

Sponsors

INDIRA GANDHI INSTITUE OF MEDICAL SCIENCE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Parturients of American society of Anaesthesiologists grade I&II between 18 & 35 years of age and posted for elective caesarean delivery under spinal anaesthesia

Exclusion criteria

Exclusion criteria: Risk of excessive bleeding. Pre-existing and pregnancy induced hypertension. Cardiovascular disease. Cerebrovascular disease.

Design outcomes

Primary

MeasureTime frame
to find out optimum dose of phenylephrine to maintain hemodynamic stability without compromising cardiac outputTimepoint: 0 , 1 , 5 minutes

Secondary

MeasureTime frame
dose of vasopressor , fetal statusTimepoint: at interval of 0,1,5 minutes

Countries

India

Contacts

Public ContactDr Pankaj Kumar

Indira Gandhi Institute of Medical Science,Patna

Secrecy143@gmail.com07979090084

Outcome results

None listed

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