Comparison of the efficacy of non-invasive skin stapler and disposable skin stapler in orthopedic surgical incision: a randomized controlled trial.

Comparison of the efficacy of non-invasive skin stapler and disposable skin stapler in orthopedic surgical incision

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000035158

Enrollment

Unknown

Registered

2020-08-02

Start date

2020-08-01

Completion date

Unknown

Last updated

2020-08-03

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

Conditions

The orthopaedic incision

Interventions

Group A:Noninvasive skin sutures incisions

Group B:Disposable skin stapler

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) The proposed line of orthopedic surgery and patients with incision for I class; 2) Aged 18 -70 years; 3) Male or female; 4) The patient agrees to participate in the trial and signs the informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients with systemic chronic wasting diseases such as hyperthyroidism, diabetes, and malignant tumors; 2) Patients with vasculogenic diseases or skin diseases such as vasculitis, varicose veins, deep venous thrombosis and psoriasis at the surgical site; 3) Patients with local or systemic infection; 4) Scar constitution; 5) Long-term use of immunosuppressants, cytoinhibitors, hormone anticoagulants and other drugs; 6) Patients with previous surgical history in the surgical area; 7) Patients with connective tissue diseases such as rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE); 8) Severe liver and kidney dysfunction, cardiovascular and cerebrovascular diseases; 9) Those suffering from neuropsychiatric diseases and unable to cooperate with the treatment; 10) Abnormal coagulation function; 11) The presence of other diseases or conditions known to affect wound healing.

Design outcomes

Primary

Measure	Time frame
First grade wound healing rate;Incision suture rate;?????;Incidence of incision dehiscence;Incidence of inflammatory reactions (redness and swelling) to the incision;The incidence of inflammatory exudate at the incision;The incidence of margin necrosis of incision;Incidence of local anaphylaxis at the incision;The degree of incision pain 1 week after operation;The degree of pain when the stapler is removed;The aesthetic degree of incision 3 months after operation;Patient satisfaction;	—

Measure

Time frame

First grade wound healing rate;Incision suture rate;?????;Incidence of incision dehiscence;Incidence of inflammatory reactions (redness and swelling) to the incision;The incidence of inflammatory exudate at the incision;The incidence of margin necrosis of incision;Incidence of local anaphylaxis at the incision;The degree of incision pain 1 week after operation;The degree of pain when the stapler is removed;The aesthetic degree of incision 3 months after operation;Patient satisfaction;

—

Countries

China

Contacts

Public ContactGou Yongsheng

Chengdu Shuangliu District First People's Hospital

15002828117@qq.com+86 15002828117

Outcome results

None listed

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