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Assessment of Circulating Fubctional Mitochondrias in Vitiligo Patients

Assessment of Circulating Fubctional Mitochondrias in Vitiligo Patients as Compared to Controls

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05525741
Acronym
MFC
Enrollment
59
Registered
2022-09-02
Start date
2022-10-19
Completion date
2025-06-30
Last updated
2024-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Skin and Connective Tissue Diseases

Brief summary

To compare the level of circulating functional mitochondria in the serum of vitiligo patients as compared to controls

Interventions

OTHERNon segmental vitiligo

The subjects will be selected from among those presenting for the consultation or hospitalization of the Dermatology department of the CHU de Nice. All necessary information will be given to the subjects and a briefing note will be given to them. A reflection period will be left for the subjects to sign the informed consent, and if necessary, another appointment will be scheduled for the inclusion visit. The Investigator: * Inform the subject of the goals, constraints and risks of the study and obtain written consent. * Conduct an examination of the subject's medical history Will verify that the subject meets all inclusion criteria and does not present any of the criteria for not including. If the subject consents and they meet all the criteria a 20 ml blood sample will be taken.

OTHERHealth Volunteers

The subjects will be selected from among those presenting for the consultation or hospitalization of the Dermatology department of the CHU de Nice. The family control subjects will be recruited from the vitiligos patients coming into our department. All necessary information will be given to the subjects and a briefing note will be given to them. A reflection period will be left for the subjects to sign the informed consent, and if necessary, another appointment will be scheduled for the inclusion visit. The Investigator: * Inform the subject of the goals, constraints and risks of the study and obtain written consent. * Conduct an examination of the subject's medical history Will verify that the subject meets all inclusion criteria and does not present any of the criteria for not including. If the subject consents and they meet all the criteria a 20 ml blood sample will be taken.

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Patients with non segmental vitiligo compared to healthy volunteers (1st degree family of vitiligo patients) atopic dermatitis, psoriasis and alopecia areata patients

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients with non segmental vitiligo, * atopic dermatitis, psoriais, alopecia areata, * 1st degree relative of vitiligo patients.

Exclusion criteria

* segmental or mixed vitiligo, * personnal history of other autoimmune disorders, * oral use of antioxidant, * pregant women

Design outcomes

Primary

MeasureTime frameDescription
Total number of circulating functionnal mitochondria (CFM) in the plasmaat baselineLevel of CFM in vitiligo serum as compared to controls

Secondary

MeasureTime frameDescription
measuring the functionality of circulating mitochondriaAt baselineFunctional analysis of CFM in vitiligo patients as compared to controls analyzed by MFI Mito Tracker

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026