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A prospective controlled study for multi-dose tranexamic acid in maintaining peri-operative hemostasis in posterior lumbar fusion surgery

Efficacy and safety of multi-dose intravenous tranexamic acid for hemostasis in posterior lumbar fusion

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038176
Enrollment
Unknown
Registered
2020-09-12
Start date
2020-09-10
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

lumbar degenerative disease

Interventions

Group A:saline 30 min preoperative iv.
Group B:Tranexamic acid: 20mg/kg preoperative iv.
group C:Tranexamic acid (20mg/kg 30min preoperative + 10mg/kg 3h after surgery)

Sponsors

Department of Orthopedics, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients Diagnosed with lumbar degenerative diseases,such as lumbar disc herniation, lumbar canal stenosis and lumbar spondylolisthesis,and with indications for posterior lumbar fusion surgery. 2. Patients should Perform primary lumbar fusion , with operative level limited to 1 or 2 segments. 3. Preoperative Hb were normal; No abnormality was found in the color doppler ultrasound of the veins of both lower extremities. 4. Above the age of 40 years old.

Exclusion criteria

Exclusion criteria: 1. Coagulation and fibrinolysin disorders; 2. History of lumbar surgery, multilevel surgery; 3. Allergic to tranexamic acid.

Design outcomes

Primary

MeasureTime frame
blood loss (total blood loss, hidden blood loss, intraoperative blood loss, postoperative blood loss);Blood transfusion rate;volume of drainage (1d, 2d and 3d postoperatively);

Secondary

MeasureTime frame
complications;length of stay;ESR,CRP,IL-6;

Countries

China

Contacts

Public ContactGanjun Feng

Department of Orthopedics, West China Hospital, Sichuan University

hx_gjfeng@126.com+86 18980606393

Outcome results

None listed

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