Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2023-01-03
2023-07-02
Brief Summary
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Researchers will compare between curcumin group and standard treatment group.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Curcuma longa oral gel group
Curcumin Gel
Curcuma longa oral gel for prevention radiation induced oral mucositis
Standard treatment group
Standard Preparation
Standard preparation for prevention radiation induced oral mucositis
Interventions
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Curcumin Gel
Curcuma longa oral gel for prevention radiation induced oral mucositis
Standard Preparation
Standard preparation for prevention radiation induced oral mucositis
Eligibility Criteria
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Inclusion Criteria
* Scheduled for 6-8 weeks of radiotherapy with 60-70Gy radiation (200cgy/fraction for 5 days/week).
Exclusion Criteria
* Any allergy to curcumin or other condiments.
16 Years
80 Years
ALL
No
Sponsors
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University of Baghdad
OTHER
Responsible Party
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sarah adnan abdul-jabbar
principal investigator
Locations
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Nuclear medicine and radiation therapy hospital
Baghdad, , Iraq
Countries
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Other Identifiers
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705722
Identifier Type: -
Identifier Source: org_study_id
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