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Role of Tranexamic acid in reducing blood loss in total hip replacement surgeries

Efficacy & Safety of two treatment regimens of Tranexamic Acid in blood sparing effect in Primary unilateral Total Hip Arthroplasties: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015421
Enrollment
126
Registered
2018-08-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M249- Joint derangement, unspecified

Interventions

Intervention1: Tranexamic Acid versus Placebo group: Group 1: 15 mg/kg of TXA in 100 ml of NS administered over a period of 10 minutes before skin incision Group 2: 15 mg/kg of TXA in 100 ml of NS ad

Sponsors

AIIMS Raipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients, 18 â?? 65 years of either sex with ASA grade I and II undergoing primary elective unilateral hip joint arthroplasty by same surgeon.

Exclusion criteria

Exclusion criteria: Patients with a) The absence of written informed consent b) Bilateral arthroplasties c) Complicated primary total hip arthroplasty with previous osteotomy, simultaneous fracture fixation, implant removal or bone grafting, History of thromboembolic diseases, d) The presence of clotting disorder or current treatment with an antiplatelet agent, anticoagulant or deep vein thrombosis (DVT) prophylaxis in the perioperative period, e) Renal disease f) History of the previous allergy to TXA. g) History of labile or uncontrolled hypertension

Design outcomes

Primary

MeasureTime frame
a. Drop in Hct after 24 hours b. Blood transfusion requirement in the first 24 hoursTimepoint: Pre-op Hb/Hct: Post-op Hb/Hct: Immediately after surgery: 24 hours after surgery: 48 hours after surgery: Drain output: 3 hours after surgery: 6 hours after surgery: 12 hours after surgery: 24 hours after surgery:

Secondary

MeasureTime frame
c. Decrease in inflammatory markers (IL6 and D-dimer) after 12 hours compared to the baseline d. Complications if any during the stay in hospital Timepoint: The Quantitative value of IL6: Before the start of surgery and 12 hours after surgery: The Quantitative value of D-dimer: Before the start of surgery and 12 hours after surgery:

Countries

India

Contacts

Public ContactSubrata Kumar Singha

AIIMS, Raipur

subratsingh@gmail.com8518881767

Outcome results

None listed

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