The State of Sexual Development in Children With Inherited Epidermolysis Bullosa
NCT05033574 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 50
Last updated 2021-09-05
Summary
The aim of the study is to determine the state of sexual development in patients with inherited epidermolysis bullosa; the study is planned to include boys and girls aged 8 to 18 years with a diagnosis of epidermolysis bullosa simplex, junctional epidermolysis bullosa, Kindler syndrome.
Conditions
- Dermatologic Disease
- Epidermolysis Bullosa
- Epidermolysis Bullosa Simplex
- Epidermolysis Bullosa Dystrophica
- Epidermolysis Bullosa, Junctional
- Kindler Syndrome
- Puberty Disorders
- Hormone Disturbance
Interventions
- DIAGNOSTIC_TEST
-
Biochemical study of hormone levels
Biochemical study of the level of follicle-stimulating hormone, luteinizing hormone, estradiol, total testosterone, prolactin, 17-hydroxyprogesterone, dehydroepiandrosterone sulfate, cortisol, insulin, thyroid-stimulating hormone, tetraiodothyronine, thyr
- DIAGNOSTIC_TEST
-
Ultrasound examination
Ultrasound examination of the pelvic organs in girls and the scrotum organs in boys
- RADIATION
-
Radiography of the hands
Determination of bone age using radiography of the hands
- BEHAVIORAL
-
Consultation of a medical psychologist
Consultation with a medical psychologist to determine the patient's psychological condition and level of intelligence
Sponsors & Collaborators
-
National Medical Research Center for Children's Health, Russian Federation
lead OTHER_GOV
Eligibility
- Min Age
- 8 Years
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-12-08
- Primary Completion
- 2021-12-01
- Completion
- 2023-06-01
Countries
- Russia
Study Locations
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