The effect of Activskin on deep partial thickness burns: a randomised control trial

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IIR-16008899

Enrollment

Unknown

Registered

2016-07-18

Start date

2016-08-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Deep partial thickness burns

Interventions

Two groups:Dressing material, a sheet of Activskin applied topically, one layer of Activskin per area of burn wound, till wound healed,once off application

versus standard dressing: normal saline cleansing and burns dressings, and paraffin gauze

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. All patients aged 18 years old and elder with two or more areas of deep partial thickness burns as defined by the LDI scanner; 2. Patient consents to having clinical photos taken; 3. Informed consent available.

Exclusion criteria

Exclusion criteria: 1. Patients who are unable to consent; 2. Infected wounds; 3. Allergy to bovine collagen; 4. Delayed presentation; 5. Pregnancy; 6. Potential patient non-compliance (refusing to follow schedule of events/follow ups).

Design outcomes

Primary

Measure	Time frame
Total healing time;	—

Secondary

Measure	Time frame
scar assessment;	—

Countries

China

Contacts

Public ContactDr sophia ko

Division of Plastic, Reconstructive and Aesthetic Surgery, Department of Surgery, Prince of Wales Hospital

sophiako@surgery.cuhk.edu.hk+852 26322639

Outcome results

None listed

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