Effectiveness and safety of different suture materials and methods in incision closure during joint replacement

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100046442

Enrollment

Unknown

Registered

2021-05-15

Start date

2021-06-01

Completion date

Unknown

Last updated

2022-01-04

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

Conditions

Joint disease

Interventions

Group 1:Subcutaneous tissue suture

Group 2:Suture on the skin surface

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing initial joint replacement; 2. Aged 18-75 years; 3. Physical and mental health, able to participate in and cooperate with the experiment; 4. No trauma or infection at the surgical site; 5. The patient is willing to participate in the study and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of multiple operations at the surgical site; 2. Allergic to the suture material in the test; 3. Patients with scar constitution; 4. Patients with poor blood pressure or blood sugar control; 5. Severe malnutrition; 6. Rheumatoid diseases, connective tissue diseases and other immunodeficiency diseases; 7. Hemophilia, vascular disease of the affected limb; 8. Obese patients with BMI>35; 9. Patients take corticosteroid drugs, anticoagulant drugs, immunosuppressive drugs and other drugs orally.

Design outcomes

Primary

Measure	Time frame
Wound complications;HWES and POSAS scoring;Suture time per wound length;	—

Secondary

Measure	Time frame
Wound suture cost;Length of stay;	—

Countries

China

Contacts

Public ContactNi Ming

PLA General Hospital

niming301@163.com+86 13581915896

Outcome results

None listed

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