Efficacy of intravenous tranexamic acid administration for Hybrid CWHTO :a randomized control trial

Efficacy of intravenous tranexamic acid administration for Hybrid CWHTO :a randomized control trial - Efficacy of intravenous tranexamic acid administration for Hybrid CWHTO :a randomized control trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000034824

Enrollment

Registered

2018-11-10

Start date

2019-02-26

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Osteoarthritis of the knee,avascular necrosis

Interventions

Intravenous tranexamic acid group: Patients received 1000 mg of tranexamic acid administered intravenously just before skin incision and 6 hours after the first intravenous administration of tranexam

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients undergoing unilateral Hybrid Closed wedge tibial osteotomy

Exclusion criteria

Exclusion criteria: 1.Patients scheduled for Hybrid Closed wedge high tibial osteotomy combined with implant removal. 2.Patients who had allergy for tranexiamic acid

Design outcomes

Primary

Measure	Time frame
The volume of perioperative blood loss measured using the calculated blood volume and change in hemoglobin from preoperative to postoperative day 3	—

Secondary

Measure	Time frame
1. The volume of perioperative blood loss measured using the calculated blood volume and change in hemoglobin from preoperative to postoperative day 7 2. Total postoperative drainage volume 3. Knee circumference at postoperative day 7 4. Complication	—

Countries

Japan

Contacts

Public ContactTakuya Iseki

Hyogo College of Medicine Orthopaedic Surgery

takuyaiseki@gmail.com0798456111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026