Trial pipeline · NCT05177289
Photobiomodulation Therapy in the Prevention and Management of Chemotherapy-Induced Alopecia
Not applicable Recruiting status last verified 2023-09
A registered clinical trial, reproduced from its ClinicalTrials.gov record. Every value on this page is a field on that record. Nothing on this page is a finding, an assessment or a recommendation.
The registered record
- Accession number
- NCT05177289
- Lead sponsor
- Jessa Hospital (other)
- Registered condition naming hair loss
- Chemotherapy-induced Alopecia
- Official title
- Evaluating the Feasibility and Efficacy of Photobiomodulation Therapy in the Prevention and Management of Chemotherapy-induced Alopecia: a Randomized Controlled Trial
Interventions
- DeviceTheradome® LH80 pro
- DeviceScalp cooling
Names and types as registered. The sponsors' free-text descriptions of these interventions are not reproduced: they are written by the party with an interest in the result, and reprinting them inside this site's layout would lend them this site's voice.
Design
- Study type
- interventional
- Phase
- Not applicable
- Allocation
- randomized
- Masking
- single
- Primary purpose
- prevention
- Enrolment
- 72 participants (estimated)
- Sites
- 1 location in Belgium
What it measures
Hair thickness measurement
Time frame: Baseline
Hair thickness measurement
Time frame: Halfway into their chemotherapy (An average of 6 weeks)
Hair thickness measurement
Time frame: At the final chemotherapy session (An average of 12 weeks)
Hair thickness measurement
Time frame: One month post chemotherapy
CTCAE-score
Time frame: Baseline
CTCAE-score
Time frame: Halfway into their chemotherapy (An average of 6 weeks)
CTCAE-score
Time frame: At the final chemotherapy session (An average of 12 weeks)
CTCAE-score
Time frame: One month post chemotherapy
Primary outcome measures only, as registered. What a trial chose to measure, and when, is the most informative thing about it that is knowable before it reports — a hair-count endpoint at 24 weeks and a patient-satisfaction endpoint at 12 weeks are not the same study.
Who can take part
- Sex
- female
- Age
- 18 Years
- Healthy volunteers
- not accepted
A summary of three registered fields, not the eligibility criteria. The full inclusion and exclusion criteria, the recruiting sites and the study contacts are on the registry record, which is the only place they are maintained. This site has no relationship with this trial and cannot refer anyone to it.
Registered dates
- Study start
- 28 February 2022 (actual)
- Primary completion
- January 2025 (estimated)
- Study completion
- January 2030 (estimated)
- First posted
- 4 January 2022 (actual)
- Last update posted
- 29 September 2023 (actual)
"Estimated" and "actual" are the registry's own labels: an estimated date is a plan, and plans move. A date is printed at the precision it was registered at: a primary completion registered as 2025-01 is a month, and rendering it as 1 January 2025 would invent a day the sponsor did not register.
Results
This trial has not reported results. ClinicalTrials.gov holds no results record for it. That is the ordinary state of a trial that is running or about to run, and it means there is nothing here to tell you about whether the intervention works — including nothing negative. If this page implied otherwise it would be wrong.
On this site
Guides covering the condition this trial is registered for. They are about published evidence; this page is about a registration, and the two do not overlap.
Chemotherapy Hair Loss: Which Drugs Cause It, What Scalp Cooling Achieves, and the Regrowth Timeline
Where this came from
Read from the ClinicalTrials.gov API on 6 September 2026 and rebuilt into this page without alteration. ClinicalTrials.gov is a service of the U.S. National Library of Medicine and is the authority on this record; where this page and the registry disagree, the registry is right. This page is not affiliated with or endorsed by NLM or NIH, or with the sponsor of this trial.
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