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Comparison of Silvosept wound and common methods on wound irrigation of Immunobullous patients

Comparison the effect of Silvosept wound and common methods on wound irrigation of Immunobullous patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017022132641N2
Enrollment
42
Registered
2017-05-20
Start date
2017-03-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

immunobullous. Bullous disorders

Interventions

Intervention 1: Intervention group: In the intervention group, wound will be washed with Normal saline, 0.9% solution of NaCl made by Daru Darman Mahdis company. Then surface of wound will be disinf
Intervention group: In the intervention group, wound will be washed with Normal saline, 0.9% solution of NaCl made by Daru Darman Mahdis company. Then surface of wound will be disinfected with Silv
In the control group, wound will be washed with Normal saline, 0.9% solution of NaCl made by Daru Darman Mahdis company. Then surface of wound will be disinfected by traditional method, like anti-bact

Sponsors

ChitoTech (Keifiat Tolid Takapoo)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients who are satisfied to enter the study, Patients with infected wounds, Hospitalized patients, Patients with age above 18 years. Exclusion criteria: Patients with skin disease such as Lupus Erythematosus and any allergic skin disease.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Microbial Count. Timepoint: After intervention. Method of measurement: Questionnaire.;Side Effects. Timepoint: After intervention. Method of measurement: Questionnaire.;Consent of patient. Timepoint: After intervention. Method of measurement: Questionnaire.;Wound healing. Timepoint: After intervention. Method of measurement: Questionnaire.;Hospitalization duration. Timepoint: After intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzaneh NayebHabib

ChitoTech Inc

fnh@aut.ac.ir+98 21 8832 1517

Outcome results

None listed

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