Skip to content

Efficacy of Intramedullary Tranexamic Acid in Elderly patients with Intertrochanteric Hip Fracture Treated by Proximal Femoral Antirotation Nail

Efficacy of Intramedullary Tranexamic Acid in Elderly patients with Intertrochanteric Hip Fracture Treated by Proximal Femoral Antirotation Nail

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260515002
Enrollment
56
Registered
2026-05-15
Start date
2024-04-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Intertrochanteric Hip Fracture Tranexamic Acid Fracture Fixation Intramedullary Intertrochanteric Fractures Blood Loss Surgical Hip Fractures Aged Randomized Controlled Trial Postoperative Hemorrhage Drug Delivery Systems Injections Saline Solution Treatment Outcome

Interventions

2 grams of Tranexamic acid injected into femur intramedullary canal after proximal reaming.,40 mL of saline injected into femur intramedullary canal after proximal reaming.
Experimental Drug,Placebo Comparator Drug
Tranexamic acid injection,Placebo

Sponsors

Research and International Relations Division, Faculty of Medicine, Srinakharinwirot University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Eligible participants were patients aged 60 years or older with a closed intertrochanteric femoral fracture (AO/OTA 31-A) deemed amenable to closed reduction and fixation with a PFNA. 2. American Society of Anesthesiologists (ASA) physical status of I to III.

Exclusion criteria

Exclusion criteria: 1. Known allergy to tranexamic acid. 2. History of myocardial infarction, cerebrovascular accident, deep vein thrombosis, pulmonary embolism, chronic liver disease, or any metabolic disease that would alter coagulation. 3. High risk of venous thrombo-embolism as estimated by Wells' score. 4. Chronic warfarin use.

Design outcomes

Primary

MeasureTime frame
Total blood loss 48 hours after intervention milliliters

Secondary

MeasureTime frame
Hidden blood loss 48 hours after intervention milliliters ,Allogeneic packed red cell transfusion During admission number of units transfused ,Post-operative haemoglobin and haematocrit 48 hours after intervention g/dL, %,30-day complications 30 days postoperative Events

Countries

Thailand

Contacts

Public ContactWittawat Boonyanuwat

Srinakharinwirot University

aofwittawat@gmail.com0839168989

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026