- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07563036
JAK2 Expression in Androgenetic Alopecia Before and After Topical Minoxidil
25. april 2026 oppdatert av: heba ahmed abdelgayed ibrahim, Kasr El Aini Hospital
Assessment of Janus Kinase 2 Expression in Patients With Androgenic Alopecia and Its Modulation by Topical Minoxidil Therapy.
Androgenetic alopecia is a common form of progressive hair loss.
This prospective single-arm pre-post interventional study aims to assess tissue Janus Kinase 2 (JAK2) expression in patients with androgenetic alopecia by comparing balding and non-balding scalp at baseline, and to evaluate changes in JAK2 expression in balding scalp after 3 months of topical minoxidil 5% therapy.
Clinical response will be assessed using standardized trichoscopic parameters.
Studieoversikt
Status
Rekruttering
Detaljert beskrivelse
This study will recruit 25 adult patients aged 18 to 50 years with mild to moderate androgenetic alopecia attending the Dermatology outpatient clinic, Cairo University Hospital.
At baseline, participants will undergo clinical evaluation, standardized photography, and trichoscopic assessment.
Three 2 mm scalp punch biopsies will be obtained over the course of the study: one from the balding scalp area and one from the non-balding scalp area at baseline, and one from the balding area after 3 months of therapy.
Tissue JAK2 protein levels will be measured by ELISA.
Participants will receive topical minoxidil 5% solution for 3 months (1 cc twice daily for men and once daily for women).
The primary endpoint is the comparison of tissue JAK2 levels between balding and non-balding scalp at baseline.
Secondary analyses will assess change in JAK2 levels after treatment and correlations with clinical improvement by trichoscopy.
Studietype
Intervensjonell
Registrering (Antatt)
25
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Heba Ahmed
- Telefonnummer: +201016532351
- E-post: heba.a.abdelgayed@kasralainy.edu.eg
Studiesteder
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Cairo Governorate
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Cairo, Cairo Governorate, Egypt, 11555
- Rekruttering
- Kasr El Aini Hospital
-
Ta kontakt med:
- Heba Ahmed, Lecturer of Dermatology
- Telefonnummer: +201016532351
- E-post: drhebaahmedyt@gmail.com
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Ja
Beskrivelse
Inclusion Criteria:
- Male adults aged 18 to 50 years with androgenetic alopecia.
- Mild to moderate disease severity, defined as Hamilton-Norwood scale II to V.
- Patients who are treatment-naive or willing to undergo an adequate washout period for prior hair loss therapies of at least 1 month.
- Willing and able to provide written informed consent.
Exclusion Criteria:
- Other types of hair loss, including inflammatory or scarring alopecia.
- Inflammatory scalp dermatoses, such as psoriasis or seborrheic dermatitis.
- Use of systemic immunosuppressants, JAK inhibitors, or systemic corticosteroids within the last 12 months.
- History of severe systemic disease, including renal, cardiovascular, or hepatic disease.
- Chemotherapy during the last 5 years.
- Bleeding disorders.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: Topical Minoxidil 5% With Scalp Biopsy and JAK2 Assessment
Participants with androgenetic alopecia will undergo baseline clinical and trichoscopic assessment, baseline 2 mm punch scalp biopsies from balding and non-balding areas for tissue JAK2 protein measurement by ELISA, treatment with topical minoxidil 5% for 12 weeks, and a repeat 2 mm punch biopsy from the balding scalp after treatment for repeat JAK2 assessment.
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Topical minoxidil 5% solution applied to the affected scalp areas for 12 weeks.
Men will apply 1 cc twice daily and women will apply 1 cc once daily.
Three 2 mm punch biopsies will be obtained during the study: one from the balding scalp area and one from the non-balding scalp area at baseline, and one from the balding scalp area after 12 weeks of treatment.
Tissue samples obtained from scalp punch biopsies will be analyzed for Janus Kinase 2 (JAK2) protein levels using ELISA at baseline and after 12 weeks of treatment.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Baseline Difference in Tissue JAK2 Protein Levels Between Balding and Non-Balding Scalp
Tidsramme: Baseline
|
Comparison of tissue Janus Kinase 2 (JAK2) protein levels measured by ELISA in scalp biopsy specimens obtained at baseline from the balding area (vertex) and the non-balding area (occipital scalp) of participants with androgenetic alopecia.
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Baseline
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Change in Tissue JAK2 Protein Levels in Balding Scalp After 12 Weeks of Topical Minoxidil
Tidsramme: Baseline to Week 12
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Change in tissue Janus Kinase 2 (JAK2) protein levels measured by ELISA in scalp biopsy specimens obtained from the balding scalp area at baseline and again after 12 weeks of topical minoxidil 5% treatment.
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Baseline to Week 12
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Change in Trichoscopic Hair Parameters After 12 Weeks of Treatment
Tidsramme: Baseline to Week 12
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Change in trichoscopic parameters from baseline to Week 12, including hair density, terminal hair density, vellus hair density, average hair thickness, follicular unit density, percentage of single, double, and triple-or-more hairs per follicular unit, and average number of hairs per follicular unit.
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Baseline to Week 12
|
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Correlation Between Change in Tissue JAK2 Levels and Clinical Response
Tidsramme: Week 12
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Correlation between the change in tissue JAK2 protein levels after treatment and the degree of clinical improvement assessed by trichoscopic parameters and baseline clinical characteristics.
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Week 12
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
1. februar 2026
Primær fullføring (Antatt)
1. oktober 2026
Studiet fullført (Antatt)
1. januar 2027
Datoer for studieregistrering
Først innsendt
25. april 2026
Først innsendt som oppfylte QC-kriteriene
25. april 2026
Først lagt ut (Faktiske)
1. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
1. mai 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
25. april 2026
Sist bekreftet
1. april 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- MS-655-2025
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
IPD-planbeskrivelse
Individual participant data (IPD) will not be shared because this is a single-center study with a small sample size, and de-identification cannot be fully guaranteed.
Aggregate results, including summary statistics and outcome analyses, will be made available through publication
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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