Compression Headband Use to Prevent Hair Loss During Whole Brain Radiotherapy
- Conditions
- Alopecia
- Interventions
- Device: Compression HeadBand
- Registration Number
- NCT02935569
- Lead Sponsor
- Michael Milano, MD,PhD
- Brief Summary
This study hypothesizes that in patients undergoing whole brain radiotherapy, a compression headband will decrease the percentage of patients with significant hair loss following radiation.
- Detailed Description
This is a pilot feasibility study. The primary objective of this study is to seek preliminary information to answer the following question:
1. Does a compression headband, placed only at the time of irradiation, reduce the incidence of significant hair loss after whole brain radiation, as compared to historical controls?
This study will also seek to answer these secondary questions:
2. Is a temporary compression headband well tolerated in patients undergoing whole brain radiation?
3. If a portion of patients do have significant hair loss after radiation in spite of compression banding, what is the timing of hair regrowth?
4. In normal volunteers, does a compression headband cause acute hypoxia in the scalp, as measured by a transcutaneous oxygen pressure monitor, and, if so, to what degree?
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 4
- Age greater than or equal to 18 years old.
- Undergoing whole brain radiation therapy, using lateral opposed fields
- Total planned radiation prescription dose between 30 Gy and 37.5 Gy in 10 to 15 treatments.
- Current complete or near-complete alopecia (natural or chemotherapy-induced)
- Concurrent or sequential chemotherapy with an agent known to commonly cause alopecia (Adriamycin, Cytoxan, Ifosfamide, Taxol (greater than 50 mg/m2), or Vincristine).
- Previous Radiation to the Scalp
- Any active dermatologic disease affecting the scalp, or temporal arteritis
- History of severe headaches.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Compression Headband Compression HeadBand a compression headband, placed only at the time of irradiation
- Primary Outcome Measures
Name Time Method Change in Hair loss defined as grade 1 (thinning or patchy) or grade 2 (complete) alopecia (hair loss), as per Common Toxicity Criteria for Adverse Effects (CTCAE) version 3 baseline to 6 weeks The primary outcome of this study will be the presence of "significant hair loss" by 6 weeks after the completion of whole brain radiation. This will be defined as grade 1 (thinning or patchy) or grade 2 (complete) alopecia (hair loss), as per Common Toxicity Criteria for Adverse Effects (CTCAE) version 3.
The amount of hair loss will be evaluated at the following time points.
* Before whole brain radiation
* six weeks following radiation
- Secondary Outcome Measures
Name Time Method Temporary compression headband side effects (Nausea, Headache, Redness, Tingling) in patients undergoing whole brain radiation 6 weeks Does a temporary compression headband cause side effects in patients undergoing whole brain ? Nausea? Headache? Redness? Tingling?
Timing of hair regrowth one year If a portion of patients do have significant hair loss after radiation in spite of compression banding, what is the timing of hair regrowth?
Acute hypoxia in the scalp of normal volunteers caused by compression headband (if present, to what degree?) as measured by a transcutaneous oxygen pressure monitor 1 hour In normal volunteers, does a compression headband cause acute hypoxia in the scalp, as measured by a transcutaneous oxygen pressure monitor, and, if so, to what degree?
Trial Locations
- Locations (1)
Dept. of Radiation Oncology, University of Rochester, Med Center
🇺🇸Rochester, New York, United States