FindTrial
Sign In

A Comparative study between administration of intravenous crystalloids and intravenous phenylephrine infusion to prevent hypotension following sub-arachnoid block in patients undergoing lower segment caesarean section

A comparative study of pre-treatment between intravenous crystalloids and intravenous phenylephrine infusion to prevent hypotension following sub- arachnoid block in patients undergoing lower segment caesarean section - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074322
Enrollment
50
Registered
2024-09-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

None listed

Interventions

Intervention1: IV crystalloid and IV phenylephrine: Infusion of IV crystalloid 500ml and IV phenylephrine 100mcg.

Sponsors

Sapthagiri institute of medical sciences and research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient willing to give written informed consent 2. Patients undergoing LSCS under SAB 3. ASA Grade - 2

Exclusion criteria

Exclusion criteria: 1. Patients with co-morbidities 2. Patients with pregnancy induced hypertension, pre-eclampsia and eclampsia. 3. All patients not suitable for SAB

Design outcomes

Primary

MeasureTime frame
Serial Assessment of Blood Pressure at intervals of every 5 minutes.Timepoint: 5 minutes—

Secondary

MeasureTime frame
APGAR score of neonatesTimepoint: At 3 time intervals—

Countries

India

Contacts

Public ContactShreyavathi R

Sapthagiri Institute of medical sciences and research centre

shreyamurthy8993@gmail.com9880588325

Outcome results

None listed

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