Effect of Turmeric on Pruritus in Hemodialysis Patients
NCT ID: NCT01037595
Last Updated: 2013-05-14
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
EARLY_PHASE1
60 participants
INTERVENTIONAL
2010-09-30
2010-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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turmeric
turmeric 500 mg tid orally for 8 weeks
turmeric
turmeric 500 md tid orally for 8 weeks
turmeric
500 mg tid orally for 8 weeks
plasebo
placebo tid orally for 8 weeks
placebo
placebo 3 time orally for 8 weeks
Interventions
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turmeric
turmeric 500 md tid orally for 8 weeks
placebo
placebo 3 time orally for 8 weeks
turmeric
500 mg tid orally for 8 weeks
Eligibility Criteria
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Inclusion Criteria
* More than 18 years old
* Pruritus
Exclusion Criteria
18 Years
70 Years
ALL
Yes
Sponsors
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Shiraz University of Medical Sciences
OTHER
Responsible Party
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Maryam Pakfetrat
associated professor of shiraz Shiraz University of Medical Sciences
Locations
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Shiraz University Hemodialysis Center
Shiraz, Fars, Iran
Countries
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References
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Hercz D, Jiang SH, Webster AC. Interventions for itch in people with advanced chronic kidney disease. Cochrane Database Syst Rev. 2020 Dec 7;12(12):CD011393. doi: 10.1002/14651858.CD011393.pub2.
Other Identifiers
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3441
Identifier Type: -
Identifier Source: org_study_id
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