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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04775316
Other study ID # C2654
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date September 1, 2021
Est. completion date November 30, 2022

Study information

Verified date November 2022
Source BSN Medical GmbH
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Although, a huge number of acute wounds is treated successfully every year, Health Care Professionals (HCPs) are facing more and more problems when treating skin damages or surgical incisions: The number of patients with fragile and/or sensitive skin is highly increasing. Such patients are having a skin integrity issue, meaning the skin is vulnerable to injury, often damaged, or unable to heal. The investigational medical devices (IMDs) of the planned clinical evaluation, Leukomed® T skin sensitive and Leukomed® T plus skin sensitive have been developed for treatment of acute wounds on patients with fragile or sensitive skin to provide a reliable but skin-friendly fixation and wound care option. The primary purpose of this clinical study is the evaluation of clinical performance to stay in place up to seven days and the safety of both dressings. Further, data on wearing comfort, product handling, pain during removal and quality of life are considered as secondary outcomes. The products will be used as part of routine wound care within the scope of their intended purpose without any additional invasive or burdensome examination.


Recruitment information / eligibility

Status Terminated
Enrollment 47
Est. completion date November 30, 2022
Est. primary completion date November 28, 2022
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Men, women or diverse - = 65 years of age - Patient is mentally and physically able to participate in this study - Signed informed consent to participate in this study - Fragile skin condition - Acute wound (surgical wound or laceration), indicated for treatment with the investigational products for a time period of 7 days Exclusion Criteria: - Infection of the target wound - Alcohol or drug addiction - Known sensitivity or allergy to any component of the study product - Patients who participate in any other clinical study investigating drugs or medical devices

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Leukomed T / Tplus skin sensitive treatment
Application of sterile wound dressing.

Locations

Country Name City State
Germany Practice Degenhardt Bremen
Germany Klinikum Dortmund Dortmund
Germany orthoGroup Hamburg

Sponsors (1)

Lead Sponsor Collaborator
BSN Medical GmbH

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adhered dressing area after wear Percentage of adhered dressing area 7 days after application 7 days after dressing application
Secondary Skin damage skin damage after dressing removal 7 days after dressing application
Secondary Skin reddening Reddening of the skin 30 min after dressing removal 7 days after dressing application
Secondary Skin reactions Further skin reactions after dressing removal after 7 days
Secondary Pain assessment Pain at dressing removal 7 days after dressing application
Secondary Product Evaluation by patient Judge wearing comfort 7 days after dressing application
Secondary Product Evaluation by Health Care Professional Assessment of handling, application and and re-application at application day (day 0)
Secondary Infection Assess signs of wound infection 7 days after dressing application
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