Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

Using light therapy to prevent hair loss from chemotherapy

Official title: Evaluating the Feasibility and Efficacy of Photobiomodulation Therapy in the Prevention and Management of Chemotherapy-induced Alopecia: a Randomized Controlled Trial

Run by Jessa Hospital · NCT05177289 · Data updated 2026-11-12

This study is testing if light therapy can help prevent hair loss in women undergoing chemotherapy for breast and gynecological cancers.

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment72 (estimated)
SponsorJessa Hospital
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Hasselt, Limburg)
StatusRecruiting
StartedFebruary 28, 2022
Main results expectedJanuary 2025
Study endsJanuary 2030
Registry record updatedSeptember 29, 2023
Trial IDNCT05177289 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 and older diagnosed with gynecological or breast cancer who are undergoing chemotherapy.

Probably not a fit

Patients with metastatic disease, pregnancy, or pre-existing hair loss conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effectiveness of photobiomodulation therapy (PBM) in preventing and managing chemotherapy-induced alopecia (CIA) in patients with gynecological and breast cancer. The research aims to determine if PBM can reduce the severity of hair loss associated with chemotherapy, thereby improving patients' quality of life. The therapy involves using a device that emits visible and near-infrared light to stimulate hair growth by enhancing blood flow to the scalp and promoting hair follicle metabolism. This approach is being compared to traditional scalp cooling methods, which have variable success rates.

Why it matters

Potential benefit: If successful, this therapy could significantly improve the quality of life for cancer patients by reducing the emotional and psychological impact of hair loss.

How similar studies have gone: While the use of photobiomodulation therapy is promising, the specific application for chemotherapy-induced alopecia has not been extensively tested in prior studies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Diagnosed with gynecological cancer (endometrium, cervix, ovarian or vulva) or breast cancer
* Receiving chemotherapy ((Carbo)-Taxol)
* Age ≥ 18 years
* Able to comply to the study protocol
* Able to sign written informed consent

Exclusion Criteria:

* Metastatic disease
* Pregnancy
* Active infection of the scalp
* Previous diagnosis of a hair loss condition
* Interruption of chemotherapy for more than two consecutive cycles
* Medication to stimulate hair growth (e.g., Minoxidil)
* Severe psychological disorder or dementia.
* Inability to speak and understand Dutch
* Substance abuse patients or patients with medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results as judged by the investigator
* Any condition that is unstable or could affect the safety of the patient and their compliance in the study as judged by the investigator

Where it's running

  • Jessa Hospital
    Hasselt, Limburg, Belgium
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.