Skip to content

The cocktail therapy control the blood loss and pain after total hip arthroplasty: A randomized controlled trial

The cocktail therapy control the blood loss and pain after total hip arthroplasty: A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16008175
Enrollment
Unknown
Registered
2016-03-28
Start date
2016-04-01
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

The blood loss and pain after total hip arthroplasty

Interventions

Cocktail Group:Intravenous plus topical hemostatic drugs and topical pain relievers
Control group:Topical hemostatic drugs only

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18-70 years old, sex is not limited; 2. The patients with severe osteonecrosis of the femoral head performed by primary unilateral uncemented THA; 3. All patients were required to sign an informed consent prior to participation in the study.

Exclusion criteria

Exclusion criteria: If they were more than 70 years old or made habitual use of opioids, had inflammatory joint disease, or had previous fracture of the affected hip, or alternatively, Hemostatic drugs and pain relievers was contraindicated or not technically possible. Revision surgery, bilateral joint arthroplasty, known hypersensitivity to TXA or its ingredients, active intravascular clotting disorders, and acute subarachnoid hemorrhage.

Design outcomes

Primary

MeasureTime frame
blood loss (including hidden blood loss);pain score (VAS);

Secondary

MeasureTime frame
Harris Score;Hemoglobin Change;

Countries

China

Contacts

Public ContactFuqiang Gao

China-Japan Friendship Hospital

gaofuqiang@bjmu.edu.cn+86 18901267995

Outcome results

None listed

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