Wound Heal Clinical Trial
— Split WoundOfficial title:
Influencing Wound Healing Through the Application of Hyaluronic Acid With Perfluorodecalin and Physalis Angulata Extract After Split Skin Removal From the Thigh - A Study in "Split Wound Design"
NCT number | NCT03668665 |
Other study ID # | 18-068 |
Secondary ID | |
Status | Withdrawn |
Phase | Phase 3 |
First received | |
Last updated | |
Start date | October 2018 |
Est. completion date | October 2020 |
Verified date | March 2019 |
Source | RWTH Aachen University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study will use a split wound design to investigate whether secondary wound healing can be accelerated and improved by the application of hyaluronic acid combined with perfluorodecalin and Physalis angulata extract.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | October 2020 |
Est. primary completion date | April 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility |
Inclusion Criteria: - Age between 18-90 years - Split skin removal at the thigh must be planned for the patients - Adult patients who are mentally and physically able to understand the importance and scope of the study and to follow up the study staff - Written informed consent before participating in the study Exclusion Criteria: - Patients suffering from a systemic disease (e.g. diabetes mellitus, anticoagulant therapy,...) - Patients taking immunosuppressive drugs that may affect wound healing - Patients suffering from skin diseases - Pregnant and/or lactating women. Women of childbearing age should protect themselves from potential pregnancy by adequate contraception while participating in studies. - Participation in a study may, at the investigator's discretion, present an unacceptable risk due to pre- or concomitant disease or the patient's general underlying condition. - Underage, or older than 90 years - Life span is less than six months - There is a current or past medically relevant disease or treatment that could influence the evaluation of the study - The patient has received a study medication within the last 30 days as part of another study - Simultaneous participation in another clinical intervention study - Expected lack of compliance - Alcohol or drug abuse - The patient is accommodated in an institution by official or court order - Patients in a dependent relationship or employment relationship with the sponsor, investigator, or alternate investigator |
Country | Name | City | State |
---|---|---|---|
Germany | Department of oral and maxillofacial surgery, University Hospital RWTH Aachen Aachen | Aachen | NRW |
Lead Sponsor | Collaborator |
---|---|
RWTH Aachen University |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Effect of Ready Medical Post Treatment on wound healing after split skin removal | Evaluation of the process control of wound healing (three-dimensional scans of the thigh) by surgeons and patients using questionnaire (wound assessment by "Patient and Observer Scar Assessment Scale") Patient and Observer Scar Assessment Scale: Vancouver Scar Scale, surface area; patient assessments of pain, itching, color, stiffness, thickness, relief (Score from 5 (best) to 50 (worse) |
6.5 month | |
Primary | Effect of Ready Medical Post Treatment on wound healing after split skin removal | Evaluation of the process control of wound healing (three-dimensional scans of the thigh) by surgeons and patients using questionnaire (wound assessment by "Manchester Scar Scale") Manchester Scar Scale: VAS (Visual Analog Scale) plus scar color, skin texture, relationship to surrounding skin, texture, margins, size, multiplicity (Score from 5 (best) to 18 (worse) |
6.5 month |
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