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Safety and efficiency of tranexamic acid in hip fracture patients

Safety and efficiency of tranexamic acid in hip fracture patients.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018110
Enrollment
Unknown
Registered
2018-08-31
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-09-03

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

Conditions

Hip fracture

Interventions

Group A:1g intravenous tranexamic acid in 100ml normal saline at admission and repeated at 3h interval, 1g intravenous tranexamic acid in 100ml normal saline before skin incision and repeated at 3h in
Group B:1g intravenous tranexamic acid in 100ml normal saline at admission and repeated at 3h interval, 100ml intravenous normal saline before skin incision and repeated at 3h interval.
Group C:100ml intravenous normal saline at admission and repeated at 3h interval, 1g intravenous tranexamic acid in 100ml normal saline before skin incision and repeated at 3h interval.
Group D:100ml intravenous normal saline at admission and repeated at 3h interval, 100ml intravenous normal saline before skin incision and repeated at 3h interval.

Sponsors

The Third Hospital of Mianyang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Consecutive patients with a diagnosis of hip fractures treated at our hospital by any surgical procedure; (2) Aged over 18 years; (3) Signed informed consent from the patient or legal representative.

Exclusion criteria

Exclusion criteria: (1) Allergy or any contraindication for tranexamic acid; (2) Delayed admission beyond 24h; (3) pathological fracture or open fracture; (4) Multiple fractures or trauma; (5) Discontinuation of oral anticoagulants or aspirin less than 1 week; (6) History of acute thromboembolic event (Deep Vein Thrombosis, Pulmonary Embolism, Stroke); (7) Patients at high risk of thrombosis; (8) Coagulopathy (INR > 1.4).

Design outcomes

Primary

MeasureTime frame
transfusion rate;transfusion amount;hidden blood loss;total blood loss;Hb level;Hb drop;

Secondary

MeasureTime frame
fibrinolysis index (D-Dimer, FDP);coagulation markers;length of hospital stay;hospitalization costs;

Countries

China

Contacts

Public ContactCong Xiao

The Third Hospital of Mianyang

xiaocong889900@163.com+86 13890459183

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 27, 2026