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Comparison of different dose of intravenous tranexamic acid on blood loss following cementless total hip arthroplasty: a double-blind randomized controlled trial

Comparison of different dose of intravenous tranexamic acid on blood loss following cementless total

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-14005247
Enrollment
Unknown
Registered
2014-08-08
Start date
2014-01-06
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

osteoarthritis

Interventions

Moderate Dose Group :10mg/kg dose of tranexamic acid
High Dose Group:15mg/kg dose of tranexamic acid

Sponsors

Shanghai Changzheng Hospital
Lead Sponsor

Eligibility

Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: (1) To be aged older than 18; (2) patients with DDH and/or OA on hip joint; (3) patients undergoing selective operation of cementless total hip arthroplasty; (4) patients who have signed informed consent.

Exclusion criteria

Exclusion criteria: (1) To be aged older than 80; (2) patients with a history of deep vein thrombosis or embolism; (3) patients with a history of drug sensitivity; (4) patients with anemia; (5) patients with a history of coagulopathy or thrombocytopenia; (6) patients with a history of hepatic or renal failure as well as severe chronic heart failure; (7) patients with a history of neurological or cerebrovascular disease; (8) patients with a history of well as those with a hip surgery previously; (9) patients with other reasons that should be excluded.

Design outcomes

Primary

MeasureTime frame
Intraoperative blood loss;Hb reduction of day 1;Actual blood loss;Post-operative blood loss;Transfusion volume;Hb reduction on day 5;

Secondary

MeasureTime frame
operating time;

Countries

China

Contacts

Public ContactFu Peiliang
fupeiliang@163.com+86 13636377844

Outcome results

None listed

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