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Low Level Laser Therapy for Hair Preservation With Chemotherapy for Breast Cancer

Low Level Laser Therapy for Hair Preservation With Chemotherapy for Breast Cancer

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01081106
Enrollment
0
Registered
2010-03-05
Start date
Unknown
Completion date
Unknown
Last updated
2012-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Breast Cancer

Brief summary

The purpose of this study is to see whether low level laser therapy can help maintain normal hair growth on the scalp in people receiving chemotherapy, which is generally associated with hair loss.

Detailed description

Chemotherapy is a common treatment given to patients with breast cancer. Many chemotherapy drugs cause rapid hair loss. While hair loss is temporary, this side effect is a significant concern for patients. Low level laser therapy has been shown to help make hair grow. It is hoped that it may stop hair loss from occurring. Participants will be receiving 20 to 30 minute laser sessions to their scalp twice a week beginning two weeks before treatment begins until one week past the last chemotherapy session. . Photographs will be taken during each study participant's initial visit, during treatment visits, and one month following the final chemotherapy treatment.

Interventions

PROCEDURELow-Level Laser Therapy

A LLLT device at 670 nm will be used for light application using lasers affixed in a rotating helmet apparatus. Treatment will be given twice weekly prior to commencing chemotherapy and will be administered once a week until one week after the last chemotherapy. administration.

Sponsors

Robert H. Lurie Cancer Center
CollaboratorOTHER
Northwestern University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participants must have breast cancer and must be starting chemotherapy with Adriamycin or a taxane-based therapy. * Participants must be 18 years old or older * Participants must be female * Participant must agree to comply with therapeutic and follow-up schedule. * Patient must signed informed consent form.

Exclusion criteria

* Participants cannot have sensitivity to the laser light. * Participants cannot have used any topical or oral products to grow hair within 3 months of enrollment to this study. * Participants cannot be pregnant, lactating or planning on pregnancy during therapeutic schedule.

Design outcomes

Primary

MeasureTime frameDescription
10 Point Scale to evaluate hair lossPhotographs evaluated weekly during treatment, one month post chemotherapyThe primary objective is to evaluate the ability of Low-Level Laser Therapy (LLLT) to prevent chemotherapy induced alopecia in women receiving adjuvant chemotherapy for breast cancer.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026