Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT05775328 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Treatment of Hypertrichosis With Intense Pulsed Light

StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary completion date: Dec 1, 2025 to Dec 1, 2026
    • Study completion date: Jul 1, 2026 to Jul 1, 2027
    v4
  2. Trial status: Not Yet Recruiting to Recruiting
    • Site details revised
    v3
  3. Study description shortened, about 13 wordsv2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this observational cohort study is to investigate the effect of intense pulsed light (IPL) for excessive hair in patients \>18 years of age and in need of gender affirmative treatment, refered to the department of dermatology and venereology, Umeå University Hospital, Sweden. The main questions this study aims to answer are: * \[To evaluate the effect of consecutive IPL treatments in women with hirsutism due to polycystic ovarial syndrome (PCOS), with or without anti-androgen treatment\] * \[To evaluate the effect of consecutive IPL treatments in individuals born as biologically men but in transition to become women, with or without hormonal treatment\]. Patients will use self-assessed questionnaires evaluating: * Background characteristics and time spend on concealing, reducing and treating hypertrichosis at home. * Ferriman-Gallwey scale, regarding the intensity of their hypertrichosis. * Dermatology Life Quality Index (DLQI) for quality of life Patients will be recruited consecutively and assessed at each visit, at the clinic before the treatments, ranging from baseline to a minimum of 5 treatment sessions.Since this is an observational study, all patients are treated by others than the researchers according to the routines och the clonic and there will be no other groups to compare the patients with.
Trial Details
NCT Number NCT05775328
Lead Sponsor Alexander Shayesteh
Conditions
(from sponsor)		 Hypertrichosis, Hirsutism - Hypertrichosis
Related terms Hirsutism, Hypertrichosis
Enrollment 39 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov