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A randomized, controlled, non-inferiority study of silver sulfate gauze self-adhesive dressings for non-chronic wounds

A randomized, controlled, non-inferiority study of silver sulfate gauze self-adhesive dressings for non-chronic wounds

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024140
Enrollment
Unknown
Registered
2019-06-27
Start date
2019-07-01
Completion date
Unknown
Last updated
2019-07-01

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

Conditions

non-chronic wounds

Interventions

Experimental group:Silver sulfate gauze self-adhesive dressing
Control group:Nano-silver trauma patch

Sponsors

The Second People's Hospital of Shenzhen
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years; 2. Patients with non-chronic wounds; 3. Patients volunteered to participate in clinical trials, and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of allergy to any form of silver; 2. Patients with severe complications of heart, liver, kidney and blood system; 3. Patients with severe complications and severe systemic infections; 4. Pregnant or lactating women; 5. Patients with poor compliance or who are in critical condition and are unable to complete the course of treatment; 6. The researchers considered the patients unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
the healing time of the wound;—

Countries

China

Contacts

Public ContactLiu lijun

The Second People's Hospital of Shenzhen

1239346224@qq.com+86 15521093884

Outcome results

None listed

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