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Topical zinc oxide in pressure ulcer

Design and clinical assessment the effect of topical formulation of zinc oxide on the healing incides of grade 1 and 2 pressure ulcers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221023056276N1
Enrollment
60
Registered
2022-12-20
Start date
2022-12-22
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

?Stage I or II pressure ulcers. Decubitus ulcer and pressure area

Interventions

Intervention 1: Intervention group: Using 10% Zinc oxide cream with cold cream base, once daily, for 14 days. Intervention 2: Control group: Using wound dressing , once daily, for 14 days.

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients with baseline stage I or II pressure ulcers according to the 2-digit Stirling pressure ulcer severity scale Patients hospitalized in Shahid Beheshti hospital, Hamedan

Exclusion criteria

Exclusion criteria: Patients with baseline stage III or IV pressure ulcers Patients with acute confirmed infection Patients with suspected ulcer Infection Patients with hypersensitivity reactions to our topical Formulations Patients who were unwilling to enter the study

Design outcomes

Primary

MeasureTime frame
The percentage of wound size change on the 7th and 14th days of the intervention. Timepoint: Measurement of wound surface area at the beginning of the study (before the start of the intervention) and 7 and 14 days after starting the intervention. Method of measurement: Imaging the surface of the wound with a camera and then calculating its area in ImageJ software.

Secondary

MeasureTime frame
The number of patients without erythema around the wound. Timepoint: At the beginning of the study (before the start of the intervention) and 7 and 14 days after starting the intervention. Method of measurement: Visual observation.;The number of cases with complete wound healing. Timepoint: Days 7 and 14 after the start of the intervention. Method of measurement: Measuring the surface area of the wound at the beginning of the study (before the start of the intervention) and 7 and 14 days after its start and observing cases of more than 90% reduction in the size of the wound compared to the dimensions measured at the beginning of the study.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRayehe Fadaie

Hamedan University of Medical Sciences

rayehe.rs@gmail.com+98 938 319 2782

Outcome results

None listed

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