Skip to content

A randomized, double-blind, placebo-controlled, clinical study evaluating the efficacy and safety of Clioquinol cream in the treatment of balanoposthitis

A randomized, double-blind, placebo-controlled, clinical study evaluating the efficacy and safety of Clioquinol cream in the treatment of balanoposthitis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034813
Enrollment
Unknown
Registered
2020-07-20
Start date
2020-07-30
Completion date
Unknown
Last updated
2020-07-27

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

Conditions

Balanoposthitis

Interventions

experimental group:Clioquinol cream
control group:placebo

Sponsors

The First Affiliated Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Chinese men over 18 years old; 2. The patients with balanitis were diagnosed clinically; 3. There were no other skin diseases or systemic diseases that could affect the detection; 4. Patients who have informed consent to the purpose and content of the study and can follow up as required.

Exclusion criteria

Exclusion criteria: 1. Patients who have systematically used glucocorticoids and / or immunosuppressants in the last month; 2. In recent 2 weeks, antibiotics, corticosteroids or other anti-inflammatory drugs have been used outside the prepuce glans area; 3. Underwent organ resection (kidney, lung, spleen, liver......), organ transplantation, a history of consciousness or sequelae caused by craniocerebral trauma within the past 5 years; 4. Patients with chronic diseases such as hypertension, diabetes, liver and kidney failure or receiving long-term treatment; 5. Patients with skin diseases affecting the measurement of external genitalia, such as glans cricoides, lichen sclerosus, lichen sclerosus (glans obliterans), erythematous hyperplasia, pemphigus, lichen planus, Bowen's disease, psoriasis, psoriasis, contact allergy, fixed drug eruption and other diseases in the test site; 6. Patients who are sensitive or allergic to the drugs used.

Design outcomes

Primary

MeasureTime frame
16s rRNA;

Secondary

MeasureTime frame
skin barrier function;severity score;

Countries

China

Contacts

Public ContactGao Xinghua

The First Affiliated Hospital of China Medical University

gaobarry@hotmail.com+86 13940152467

Outcome results

None listed

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