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Comparing sutures versus staples for leg wound closure after coronary artery bypass grafting: a randomized controlled trial

Comparing sutures versus staples for leg wound closure after coronary artery bypass grafting: a randomized controlled trial - HANK

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036824
Enrollment
426
Registered
2025-05-21
Start date
2023-08-16
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

I25

Interventions

Group 1: Closure of the wound with staples In a parallel-group design, wound closure following saphenectomy differs between the two study arms. In arm 1, the wound is closed using a stapling device. A

Sponsors

Uniklinik Köln, Klinik und Poliklinik für Herzchirurgie, herzchirurgische Intensivmedizin und Thoraxchirurgie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing elective or urgent CABG surgery

Exclusion criteria

Exclusion criteria: Inability to consent, material allergy

Design outcomes

Primary

MeasureTime frame
Surgical site complications within six months, defined as a composite of infection or wound healing disturbances requiring extended medical outcome. Postoperatively, regular wound inspections are performed, and local signs of infection are documented on days 1, 5, and 10. Wound assessment is conducted using a modified Hollander Wound Evaluation Scale (HWES) and the ASEPSIS score. Six months after surgery, both scores as well as the cosmetic outcome are reassessed via a follow-up telephone interview.

Secondary

MeasureTime frame
Wound scores, pain, cosmetic outcomes Postoperatively, regular wound inspections are performed, and local signs of infection are documented on days 1, 5, and 10. Wound assessment is conducted using a modified Hollander Wound Evaluation Scale (HWES) and the ASEPSIS score. Six months after surgery, both scores as well as the cosmetic outcome are reassessed via a follow-up telephone interview.

Countries

Germany

Contacts

Public ContactClara Großmann

Uniklinik Köln, Klinik und Poliklinik für Herzchirurgie, herzchirurgische Intensivmedizin und Thoraxchirurgie

clara.grossmann@uk-koeln.de0221 478 32405

Outcome results

None listed

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