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NCT07049705

Factors Influencing Bradycardia During Spinal Anesthesia in Obstetric Patients Undergoing Cesarean Section

Active, enrolled Last updated 3 July 2025
What this trial tests

trial in Cesarean Section Complications in 289 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
17 March 2025
Primary endpoint
1 September 2025
28 February 2026

Quick facts

Lead sponsorSuperior University
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment289
Start date17 March 2025
Primary completion1 September 2025
Estimated completion28 February 2026
Sites1 location across Pakistan

Conditions studied

Sponsor

Superior University

Who can join

Adults 18 to 40, any sex, with Cesarean Section Complications. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study titled "Factors Influencing Bradycardia During Spinal Anaesthesia in Obstetric Patients Undergoing Caesarean Section"" aims to investigate the causes and patterns of bradycardia in pregnant women receiving spinal anesthesia during cesarean deliveries. Bradycardia, defined as a heart rate below 60 beats per minute, is a known complication of spinal anesthesia, often resulting from sympathetic blockade and unopposed parasympathetic activity. This condition may lead to hypotension, decreased cardiac output, and compromised fetal oxygenation.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cesarean Section Complications

Currently open trials in the same condition.

Other Superior University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07049705.

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