Demonstration of the Presence of a Carbonyl Stress in the Hair Follicles of Postpartum Women (NCT04237402) | Clinical Trial Compass
CompletedNot Applicable
Demonstration of the Presence of a Carbonyl Stress in the Hair Follicles of Postpartum Women
France20 participantsStarted 2018-06-15
Plain-language summary
In this study, the investigator will try to highlight the presence of carbonyl compounds in the hair follicles of postpartum women by comparing these compounds before and after delivery.
Who can participate
Age range18 Years – 40 Years
SexFEMALE
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Inclusion Criteria:
Criteria related to the Population:
* Pregnant woman (≥ 33 weeks of amenorrhea)
* Woman aged between 18 and 40 years (included)
* Phototype I to IV included according to Fitzpatrick's classification
* Affiliation to a French social security scheme or benefiting from such a scheme
* Signed informed consent form
Exclusion Criteria:
Criteria related to the Population:
* High risk or pathological pregnancy, according to the opinion of the investigator
* Deprivation of liberty by administrative or judicial decision or subject under guardianship
* Impossibility, according to the investigator, to comply with the requirements of the protocol
* Linguistic or psychic incapacity to sign informed consent
* Concomitant participation in a clinical study that may interfere with the results of the study, according to the opinion of the investigator (excluding observational studies)
Criteria related to Pathology :
* Alopecia causing hair loss on the upper part of the scalp
* Dermatological pathology or evolving cutaneous lesion in the scalp
* Known history of hepatitis B and C, HIV
* Past or present neoplastic condition
* Acute evolving pathology
* Gestational diabetes treated with insulin
Criteria related to Treatments:
* Treatment of general thyroid disorders initiated or modified for less than 3 months prior to inclusion (or change of specialty for less than 3 months)
* Systemic treatment affecting hair growth taken for at least 4 weeks during the 3 months prio…
What they're measuring
1
Change of biological evaluation
Timeframe: 1st sample: inclusion visit (up to 8 weeks before delivery)- 2nd sample: end of study visit (10 to 16 weeks after delivery)