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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04886882
Other study ID # SakuraDermatology1
Secondary ID
Status Enrolling by invitation
Phase Early Phase 1
First received
Last updated
Start date March 22, 2021
Est. completion date July 1, 2021

Study information

Verified date April 2021
Source Basaksehir Cam & Sakura Sehir Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

An experimental study examining wound healing in 5 different groups on 30 rats.


Description:

Magnesium topically increases collagen synthesis and angiogenesis, providing faster and higher quality wound healing. In addition, with its analgesic effect, it will also eliminate the pain sensation caused by the wound and increase the quality of life of the patient whose skin integrity is impaired.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 30
Est. completion date July 1, 2021
Est. primary completion date June 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 8 Weeks to 12 Weeks
Eligibility Inclusion Criteria: - healthy rats between ages of 8- 12 weeks Exclusion Criteria: - weight loss of more than 15% of body weight

Study Design


Related Conditions & MeSH terms


Intervention

Other:
placebo comparator
solution containing 0.9 % sodium chlorine
sham comparator
vaseline, beeswax,polyglyceryl-3 diisostearate, sorbitan caprylate, propandiol,benzoic acid, glycerin, water
Experimental drug 1
A cream containing 10 % MgSO4.vaseline, beeswaxpolyglyceryl-3 diisostearate, sorbitan caprylate, propandiol,benzoic acid, glycerin, water
Experimental drug 2
A cream containing 10 % MgSO4.vaseline, beeswax,polyglyceryl-3 diisostearate, sorbitan caprylate, propandiol,benzoic acid, glycerin, water
Drug:
Centella asiatica
A cream containing Centella asiatica

Locations

Country Name City State
Turkey Basaksehir Çam Ve Sakura Hospital Istanbul

Sponsors (2)

Lead Sponsor Collaborator
Basaksehir Cam & Sakura Sehir Hospital Istanbul Kent University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary 7th day evaluation Histopathological evaluation of wound healing comparing with the rate of vascular endothelial growth factor (VEGF), transforming growth factor (TGF-beta) and hydroxyproline at immunohistochemical staining with biopsy on the 7th day. 7th day
Secondary 15th day evaluation Histopathological evaluation of wound healing comparing with the rate of VEGF, TGF-beta and hydroxyproline at immunohistochemical staining with biopsy on the 15th day. 15th day
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