CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 60 enrolled
Drug / intervention
Tranexamic Acid (TXA) +1 moredrug
Likely dose
Tranexamic Acid (TXA) 20 mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT07392034
NCT07392034Phase 2Completed

Efficacy of Tranexamic Acid Reducing Blood Loss During Maxillofacial Trauma Surgery

Nishtar Medical University·interventional·Posted Feb 6, 2026·Updated Feb 6, 2026

In Brief

A Phase 2 clinical trial evaluating Tranexamic Acid (TXA) and Normal saline for Hemoglobin Level Measurement and 2 related conditions. Completed, enrolled 60 participants across 1 site.

Detailed Summary

Tranexamic acid (TXA) is an inexpensive, easily used and relatively safe drug. It inhibits plasminogen activation and plasmin thus retards clot disintegration.Therapeutic application of tranexamic acid in trauma for preventing blood loss has been documented since long. Since blood loss causes several serious complications, it is compensated emergently by transfusion of blood or its products. However, transfusion of blood and products always carries a risk of inadvertent transmission of infection, antigen-antibody reactions and additional cost all of which can be prevented if blood loss is reduced. Morbidity associated with the delay in compensating the blood loss could also be prevented by pharmaceutically preventing hemorrhage.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesPakistan
Collaborators--

Timeline

Phase 2CompletedFinished
20252026
First PostedFeb 6, 2026
Enrollment StartJan 1, 2025
Primary CompletionJun 30, 2025
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 5 months ago

Interventions

Tranexamic Acid (TXA)drug

Thirty minutes prior to surgery, the intervention group receive intravenous , single dose of tranexamic acid of 20 mg/kg.

Normal salinedrug

Thirty minutes prior to surgery, the placebo group received single dose of 20 mL of normal saline.