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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01861782 |
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Date of registration:
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12/05/2013 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Comparison Between Dead Sea Solar and Water Treatment to Sulfur Pool and Medicinal Mud Treatment in Patients With RA
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Scientific title:
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Comparison Between Dead Sea Solar and Water Treatment to "Sulfur Pool" and Medicinal Mud Treatment in Patients With Rheumatoid Arthritis |
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Date of first enrolment:
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June 2013 |
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Target sample size:
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30 |
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Recruitment status: |
Active, not recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01861782 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Supportive Care
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Phase:
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N/A
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Countries of recruitment
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Israel
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. Male and female = 18
2. Patients with diagnosed rheumatoid arthritis
3. Patients with moderate disease activity (DAS28 > 3.2)
Exclusion Criteria:
1. Patients who suffer from Photosensitivity
2. Patients with Suspected Lupus Erythematoides
3. Patients with tendency to sudden loss of consciousness and/or dizziness
4. Patients under chemotherapeutic treatment
5. Patients with Active Malignancy
6. Patients with lowest level of physical functioning (class 4)
7. Patients with serious uncontrolled concomitant chronic disease
8. Drug Abuser
9. Patients with severe peripheral venous insufficiency
10. Pregnant women
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Rheumatoid Arthritis
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Intervention(s)
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Other: Dead Sea Solar and Water Treatment
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Other: Sulfur Pool & Medicinal Mud
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Primary Outcome(s)
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Assessing the change in DAS28 (Disease Activity Score) between the baseline and several occasions after each one of the proposed treatments.
[Time Frame: up to 4 months]
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Secondary Outcome(s)
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Assessing the change between baseline and several occasions after each one of proposed the treatments
[Time Frame: up to 4 months]
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Secondary ID(s)
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0356-12-SOR
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sor0356-12ctil
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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