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Prophylactic Tranexamic Acid To Reduce Blood Loss During Caesarean Delivery.

Prophylactic Role Of Tranexamic Acid To Reduce Blood Loss During Caesarean Delivery : A Prospective Study.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06604325
Enrollment
300
Registered
2024-09-19
Start date
2024-10-01
Completion date
2025-03-30
Last updated
2024-10-24

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

Conditions

Post Partum Hemorrhage

Brief summary

Postpartum hemorrhage continues to be the leading cause of maternal morbidity and mortality. Globally, it is responsible for 25% of all pregnancy-related deaths. PPH is unpredictable and may occur in the absence of risk factors. Tranexamic acid is an antifibrinolytic proven to reduce blood loss and transfusion requirements for various surgeries. This study aims to explore the effectiveness of tranexamic acid as an adjunct to other uterotonics before the Caesarian Section.

Interventions

DRUGTranexamic acid injection

All women recruited to Group A will receive tranexamic acid 1 gram in 100 ml Normal Saline as intravenous infusion 10 minutes before the skin incision.

DRUGPlacebo

All women recruited to Group B will receive 100 ml Normal Saline as intravenous infusion 10 minutes before the skin incision.

Sponsors

Aligarh Muslim University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

1. The women undergoing cesarean delivery (both elective and emergency) during the study period. 2. Willing to participate in the study after understanding the concept.

Exclusion criteria

1. Critically ill patient. 2. Not willing to give consent to participate in the study 3. Cases diagnosed with a ruptured uterus or undergoing caesarian hysterectomy during operation.

Design outcomes

Primary

MeasureTime frameDescription
Perioperative blood lossAmount of blood loss from starting from surgical incision till 24 hours post caesarean section.The primary aim of the trial is to investigate the effect of tranexamic acid on peri and post- operative blood loss during caesarean section

Countries

India

Contacts

Primary ContactMUAZZAM HASAN, MD
MUAZZAMSH@GMAIL.COM9808447427

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026