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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01490554
Other study ID # CEP UNIFESP-1787/07
Secondary ID
Status Active, not recruiting
Phase N/A
First received December 9, 2011
Last updated July 23, 2012
Start date March 2007
Est. completion date December 2012

Study information

Verified date July 2012
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil : Research Ethics CommitteeBrazil : ANVISA
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the presence of skin changes after grafting of autologous fibroblasts by means of biophysical, histological, immunohistological, gene expression, glycosaminoglycan, and sensitivity analyses.


Description:

- Analytical prospective autocontrolled study


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date December 2012
Est. primary completion date March 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria:

- Women, aged between 50 to 70 years with facial wrinkles (rhytides),

- Fitzpatrick III skin type, and

- Who had reached menopause at least 3 years before entering the study were eligible for participation.

Exclusion Criteria:

- Women with uncontrolled comorbid conditions,

- Smokers,

- Alcohol and corticosteroid users,

- Who had undergone chemical peeling or skin filling in the face or neck at least 12 months prior to the study,

- Who had a keloid scar,

- Who scored below 18 on the Mini-Mental State Examination,

- Who had any psychiatric disorder or those undergoing orthodontic treatment were excluded from the study.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
autologous fibroblasts grafts
Autologous cultured fibroblasts will be grafted in facial skin

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Federal University of São Paulo

Outcome

Type Measure Description Time frame Safety issue
Primary Regeneration of facial ectoderm To evaluate the presence of skin changes after grafting of autologous fibroblasts by means of biophysical, histological, immunohistological, gene expression, glycosaminoglycan, and sensitivity analyses. one year after the grafting of autologous fibroblasts. Yes
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