Use of Chamomilla Recutita in Mucositis
- Conditions
- Mucositis
- Registration Number
- NCT01341054
- Lead Sponsor
- University of Sao Paulo
- Brief Summary
To determine the Chamomilla recutita solution dose needed to reduce the intensity and evolution time of oral mucositis in adult subjects submitted to HSCT.
- Detailed Description
Population: adult subjects, submitted to hematopoietic stem cell transplantation (HSCT) at a cancer hospital in the interior of São Paulo State. The following inclusion criteria were adopted for sample selection purposes: subjects over 18 years of age, candidates for allogeneic HSCT and with intact oral cavity on the first day of conditioning. Subjects will be excluded if they present any adverse reaction to the active principles of Chamomilla recutita; receive oral or intravenous anticoagulation therapy; use oral or systemic topical anti-inflammatory medication; receive any other type of intervention for mucositis not included in the standard oral care protocol.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- subjects over 18 years of age;
- candidates for allogeneic HSCT;
- with intact oral cavity on the first day of conditioning.
- present any adverse reaction to the active principles of Chamomilla recutita;
- receive oral or intravenous anticoagulation therapy;
- use oral or systemic topical anti-inflammatory medication;
- receive any other type of intervention for mucositis not included in the standard oral care protocol.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Oral mucositis intensity The measurement will be held on the first day of the conditioning regimen to bone marrow grafting. In an expected average of 4 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hospital Amaral Carvalho
🇧🇷Jau, São Paulo, Brazil
Hospital Amaral Carvalho🇧🇷Jau, São Paulo, Brazil