Trial Comparing Best Supportive Care to Aloe Vera Gel
Phase III Trial Comparing Best Supportive Care to Aloe Vera Gel as a Prophylactic Agent for Radiation Induced Skin Toxicity
1 other identifier
interventional
137
1 country
1
Brief Summary
Radiation therapy (RT) has been a component of breast cancer treatment for almost 100 years. Although initially used for the treatment of chest wall recurrences after mastectomy and for advanced inoperable disease, RT has evolved into a critical component of early therapy for women with an intact breast following lumpectomy and for mastectomized women who are at high risk for local failure. Currently breast cancer patients need a multidisciplinary management including surgery, chemotherapy and radiotherapy, radiotherapy has a significant role in loco regional control of the disease. It is estimated that 87% of these women will develop some degree of radiation-induced dermatitis, varying from mild to brisk erythema or even moist desquamation. Topical agents, such as corticosteroid creams and other products including Aquaphor (Beirsdorf Inc, Wilton, CT), and trolamine (Biafine; Genmedix Ltd, France), are commonly prescribed at the onset of radiation dermatitis or, in some institutions, at the beginning of radiotherapy. The aim of this randomized phase III study was to assess the effectiveness of aloe vera cream for the prevention of acute radiation-induced dermatitis of grade 2 or higher during postoperative radiotherapy for breast cancer, compared to best supportive care. The secondary objectives were to assess pain, treatment interruption as a result of skin reactions, and the quantity of life during the treatment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_3
Started Mar 2007
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2008
CompletedFirst Submitted
Initial submission to the registry
April 5, 2009
CompletedFirst Posted
Study publicly available on registry
April 7, 2009
CompletedApril 7, 2009
April 1, 2009
1.5 years
April 5, 2009
April 6, 2009
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Acute radiation-induced dermatitis of grade 2 or higher during postoperative radiotherapy for breast cancer.
Secondary Outcomes (1)
quality of life,interruptions of treatment and pain.
Study Arms (2)
1
EXPERIMENTAL2
NO INTERVENTIONInterventions
The aloe vera gel which was commercially available, contained water, aloe vera, D-panthenol, triethanolamine, carbomer 934P, hyaluronic acid, potassium sorbate, diazolidinyl urea, methylparaben, and propylparaben.
Eligibility Criteria
You may qualify if:
- The women had to be 18 to 75 years of age with a nonmetastatic breast adenocarcinoma treated by either lumpectomy or mastectomy with or without adjuvant postoperative chemotherapy or hormonal treatment, and referred to the Department of Radiotherapy for postoperative radiotherapy. Concomitant chemotherapy was allowed.
You may not qualify if:
- Women with bilateral cancer, patients who were allergic to either of the two agents, and pregnant women were excluded.
- No rash, ulceration, bleeding, or unhealed scar was allowed in the treatment area.
- Patients were excluded for: prior radiation therapy (RT), mastectomy, skin involvement by tumor, history of, or current connective tissue disorder, medical contraindication (allergy or sensitivity) to Aloevera or planned BSC, and inability to comply with treatment regime. The use of bolus was prohibited.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Gustavo Viani
Marília, Sao Paulo\brazil, 17501570, Brazil
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
April 5, 2009
First Posted
April 7, 2009
Study Start
March 1, 2007
Primary Completion
September 1, 2008
Study Completion
December 1, 2008
Last Updated
April 7, 2009
Record last verified: 2009-04