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A randomized, controlled, superior-efficacy study of silver ion anorectal functional dressing for wound after hemorrhoid surgery

A randomized, controlled, superior-efficacy study of silver ion anorectal functional dressing for wound after hemorrhoid surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039169
Enrollment
Unknown
Registered
2020-10-20
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-01-18

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

Conditions

Wound after hemorrhoid operation

Interventions

treatment group:Silver ion dressing
control group:routine treatment

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients aged between 18 and 65 years old; 2. Patients who need open hemorrhoids operation; 3. The patients who agreed to participate in the trial signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of allergy to silver; 2. Patients with severe complications of heart, liver, kidney and blood system, severe complications and severe systemic infection; 3. Patients with acute metabolic disorder; 4. Patients with severe immune system diseases; 5. Pregnant and lactating women; 6. Other patients considered unsuitable by researchers.

Design outcomes

Primary

MeasureTime frame
healing time;—

Secondary

MeasureTime frame
Wound pain score;—

Countries

China

Contacts

Public ContactYang Feng

Shenzhen Second People's Hospital

1239346224@qq.com+86 13128713491

Outcome results

None listed

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