faculty of medicine-Fayoum university
Al Fayyum, 63519, Egypt
NCT Number: NCT06301178
Scars and keloids cause patients severe morbidity and psychological distress. Hypertrophic scars rise above the skin but stay within the scar boundaries, while keloids expand.
The development of keloids and hypertrophic scars is a consequence of insufficient wound healing. These lesions are distinguished by excessive ECM deposition. Excessive ECM deposition is caused by increased inflammatory and proliferative processes and decreased remodeling activities. These scarring lesions are also linked to genetic and systemic causes
Looking for future studies?
Notify Me18 year–50 year
All sexes
Interventional
Phase 1 / Phase 2
Al Fayyum, 63519, Egypt
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Age below 12 years and above 50 years. Patients received other treatment modalities for hypertrophic scars and keloids.
Systemic and other skin diseases. Patients were already receiving supplemental vitamin D.
Vitamin D has various critical regulatory roles, including inflammatory control, cellular proliferation and differentiation, and wound healing regulation.
Time frame: 3 months
Four characteristics of the scar are assessed. These are: vascularity, height, pliability, and pigmentation. Each characteristic is given a score, which are added together to give an overall score between 0 and 13
Mostafa Bahaa
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06436183
Atopic, Atopic Dermatitis
Phoenix, Arizona, United States
View Trial DetailsNCT05607901
Dermatologic Disease, Skin Diseases
Tanta, Egypt
View Trial DetailsNCT06397664
Adolescent Development, Dermatologic Disease
Oxford, United Kingdom
View Trial DetailsNCT03931226
Dermatologic Disease, Otorhinolaryngologic Diseases
Toulouse, France
View Trial Details