NCT07547488

Brief Summary

This study investigates the effect of different dressings on skin pH when applied to a simulated skin fold environment.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Nov 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 5, 2025

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

March 23, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

April 23, 2026

Completed
7 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
Last Updated

April 23, 2026

Status Verified

October 1, 2025

Enrollment Period

6 months

First QC Date

March 23, 2026

Last Update Submit

April 16, 2026

Conditions

Skin Folds

Outcome Measures

Primary Outcomes (1)

  • Difference in skin pH

    Difference in skin pH between the simulated skin fold and the area under Sorbact® Compress, measured after approximately 24 hours of wear time

    24 hours of wear time

Secondary Outcomes (3)

  • Difference in skin pH

    24 hour of wear time

  • Difference in skin pH

    24 hours of wear time

  • Change in skin hydration under occlusion from baseline

    24 hours of wear time

Other Outcomes (1)

  • Differences in skin pH between the different dressings

    24 hours of wear time

Study Arms (1)

Dressings

EXPERIMENTAL

Every participant will use all different dressing used in the trial.

Device: Dressings

Interventions

DressingsDEVICE

Sorbact® Ribbon, Sorbact® Compress and InterDry®

Dressings

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Written informed consent to participate in this study
  • Healthy men and women between 18-80 years
  • Patient is mentally and physically able to participate in this study
  • Intact skin on the forearms without any signs of irritation
  • Agreed on not to shower or use cosmetic products on the arms the same day as visit 1 and during the study period
  • Agreed not to engage in intense physical activity throughout the study period

You may not qualify if:

  • Skin disorder of any kind.
  • Known allergy to adhesives or/and any other component(silver) in the investigation devices.
  • Pregnant or lactating women.
  • Presence of tattoos on the forearms.
  • Ongoing medication with antibiotic.
  • Suffer from excessive sweating, hyperhidrosis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Essity Study site

Mölndal, Sweden

RECRUITING

MeSH Terms

Interventions

Bandages

Intervention Hierarchy (Ancestors)

Equipment and Supplies

Central Study Contacts

Fana Hunegnaw

CONTACT

+46761361512fana.hunegnaw@essity.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 23, 2026

First Posted

April 23, 2026

Study Start

November 5, 2025

Primary Completion

April 30, 2026

Study Completion

April 30, 2026

Last Updated

April 23, 2026

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations

SE(1)