Skip to content

Cluster randomised trial testing Disposable versus Reusable drApes and Gowns for green OperatiNg theatres (DRAGON)

Multicentre non-inferiority cluster randomised trial testing Disposable versus Reusable drApes and Gowns for green OperatiNg theatres

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202407689714460
Enrollment
26800
Registered
2024-07-01
Start date
2024-02-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Surgery

Interventions

Reusable drapes and gowns
Disposable single use drapes and gowns

Sponsors

The University of Birmingham
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with at least one incision that is =5cm in adults and =3cm in children aged under 16 years. This can include both open and minimally-invasive surgery providing at least one incision meets this criteria. Patients with a clean-contaminated, contaminated, or dirty surgical wound. Patients undergoing emergency (surgery on an unplanned admission) or elective (surgery on a planned admission) surgery. Any operative indication (including caesarean section). Patients aged 10 or over.

Exclusion criteria

Exclusion criteria: Adults with an incision <5 cm and incision <3cm in children aged under 16 years. Patients undergoing procedures with a clean surgical wound only.

Design outcomes

Primary

MeasureTime frame
The primary outcome is surgical site infecTIon (SSI) within 30 days of surgery, evaluated based on the US Centre for Disease Control (CDC) criteria. The day of surgery is defined as day zero. The primary outcome will be determined by a computer-based algorithm based on the CDC criteria.

Secondary

MeasureTime frame
Surgical wound related costs;Carbon footprint;Mortality and likely cause;Unplanned wound opening;Antibiotic prescribing for SSI;Reattendance at emergency department;Readmission to hospital;Reoperation for SSI;Total length of hospital stay

Countries

Benin, Ghana, Nigeria, Rwanda, South Africa

Contacts

Public ContactRachel Lillywhite

Trials Management Team Leader

r.e.lillywhite@bham.ac.uk447514800721

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026