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WithdrawnNCT01081106Updated Jul 31, 2012

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

An interventional study of Low-Level Laser Therapy in Breast Cancer, sponsored by Northwestern University. Withdrawn. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-07-31.

Sponsored by Northwestern University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Non-randomized
Ages
18 Years and older
Sex
Female
01

Study 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.

Read the 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.

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Conditions studied

  • Breast Cancer

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Keywords

  • Breast Cancer
03

In context

Breast Neoplasms

12,547 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

Browse Breast Neoplasms studies →

Lead sponsor

Northwestern University is the lead sponsor of 1,398 studies on the registry; 201 are open to participants now.

Of its 102 completed or terminated interventional studies of FDA-regulated products, 73 (72%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts 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

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.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Other
    Low-Level Laser Therapy

    Procedure: Low-Level Laser Therapy

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.

06

What researchers measure

Primary outcomes

  1. 10 Point Scale to evaluate hair loss

    The 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.

    Time frame: Photographs evaluated weekly during treatment, one month post chemotherapy

07

Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 31, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01081106
Lead sponsor
Northwestern University
Collaborators
Robert H. Lurie Cancer Center
Responsible party
Sponsor
First posted
Mar 5, 2010
Last update
Jul 31, 2012

Study contacts

Jamie Van Roenn, MD
principal investigator · Northwestern University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Jul 2012. You cannot join it, but the record below documents what was studied.

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