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Efficacy and safety of absorbable floseal in total knee arthroplasty

Efficacy and safety of absorbable floseal in total knee arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083957
Enrollment
Unknown
Registered
2024-05-08
Start date
2023-03-06
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Bone and joint disease

Interventions

Group of the fluid gelatin:use fluid gelatin on surgical site
Group of tranexamic acid:use 1g tranexamic acid on surgical site

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Patients with unilateral primary total knee arthroplasty; (2) ASA classification: 1-II1; (3) Age 18-80 years old

Exclusion criteria

Exclusion criteria: (1) Allergic to fluid gelatin; (2) Bleeding diseases and coagulation dysfunction (including various blood diseases and liver diseases, such as thrombocytopenia to <50x10?, severe liver disease caused by hepatitis B, hepatitis C and other severe liver diseases accompanied by coagulation dysfunction, etc.) are not controlled: (3) Anticoagulant drugs are currently being used, such as warfarin; (3) The orthopedic surgeon judged that there were contraindications to surgery: (4) Refusal to participate in the clinical trial.

Design outcomes

Primary

MeasureTime frame
Hb;

Secondary

MeasureTime frame
Hematocrit;Amount of blood loss during surgery;Degree of swelling;blood Drainage;score of pain;Postoperative complications;Joint range of motion;

Countries

China

Contacts

Public ContactZongke Zhou

West China Hospital of Sichuan University

zhouzongke@scu.edu.cn+86 189 8060 1028

Outcome results

None listed

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