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Comparison of Different Modes of Administration Tranexamic Acid in Reducing Post Operative Blood loss After Total Hip Replacement

Comparison of Different Modes of Administration Tranexamic Acid in Reducing Post Operative Blood loss After Total Hip Replacement:A Randomized Control Trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084566
Enrollment
102
Registered
2025-04-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: M169- Osteoarthritis of hip, unspecified

Interventions

Intervention1: TRANEXAMIC ACID: Pateints undergoing total hip arthroplasty Preoperative Hemoglobin and Hematocrit levels will be measured using Wintrobe hematocrit tube on a Hematocrit centrifuged

Sponsors

TEERTHANKAR MAHAVEER MEDICAL COLLEGE AND RESEARCH CENTRE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either gender Age more than 18 years Non Traumatic/elective cases of Primary Osteoarthritis ,Secondary Osteoarthritis of hip due to Septic Arthritis,Tuberculosis and Avasular necrosis Post Traumatic Arthritis Patient willing for participation in this study Hemoglobin level more than equal to 10gm/dl Packed Cell volume more than33%

Exclusion criteria

Exclusion criteria: Patients of either gender Age more than 18 years Non Traumatic/elective cases of Primary Osteoarthritis ,Secondary Osteoarthritis of hip due to Septic Arthritis,Tuberculosis and Avasular necrosis Post Traumatic Arthritis Patient willing for participation in this study Hemoglobin level more than equal to 10gm/dl Packed Cell volume more than33%

Design outcomes

Primary

MeasureTime frame
TO COMPARE THE EFFICACY OF DIFFERENT MODES OF TRANEXEMIC ACID IN REDUCING POST OPERATIVE BLOOD LOSS AFTER TOTAL HIP REPLACEMENT SURGERYTimepoint: 1-5th day

Secondary

MeasureTime frame
through this study we are also assessing the safety of tranexamic acidTimepoint: 0-5 days of administration

Countries

India

Contacts

Public ContactDr Amit Saraf

TEERTHANKAR MAHAVEER MEDICAL COLLEGE AND RESEARCH CENTRE

amitsaraf_75@yahoo.com09780029750

Outcome results

None listed

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