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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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12 December 2020 |
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Main ID: |
NCT02754089 |
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Date of registration:
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26/04/2016 |
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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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The Effects of Rhus Coriaria L. on Body Weight
SomaghWeight |
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Scientific title:
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The Effects of Rhus Coriaria L. (Rhus or Somagh) on Body Weight |
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Date of first enrolment:
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May 2016 |
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Target sample size:
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50 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02754089 |
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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: Parallel Assignment. Primary purpose: Treatment. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Iran, Islamic Republic of
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Contacts
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Name:
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Mojtaba Heydari, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Research Center for Traditional Medicine and History of Medicine, Shiraz University of Medical Sciences, Shiraz, IR Iran |
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Name:
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Zahra Hajmohammadi, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Department of Internal Medicine, Shiraz University of Medical Sciences, Shiraz, Iran |
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Name:
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Gholamhossein Ranjbar Omrani, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Endocrine and Metabolism Research Center, Shiraz University of Medical Sciences |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Body mass index (BMI) >= 25 kg/m2
Exclusion Criteria:
- Diabetes mellitus
- Hypo. or hyperthyroidism
- Any systemic illnesses e.g. liver cirrhosis, acute or chronic renal failure, heart
failure
- Use of drugs: Weight lowering agents, glucocorticoids, Oral contraceptive pills.
- Pregnancy
- History of allergic reaction to Somagh
Age minimum:
18 Years
Age maximum:
60 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Body Weight
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Intervention(s)
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Drug: Placebo
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Drug: Rhus Coriaria L.(Rhus)
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Primary Outcome(s)
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Body Mass Index
[Time Frame: 6 weeks]
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Secondary Outcome(s)
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Leptin (ng/ml)
[Time Frame: 6 weeks]
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Number of patients with adverse event
[Time Frame: 6 weeks]
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Fasting Blood Glucose (mg/dl)
[Time Frame: 6 weeks]
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Insulin (mU/l)
[Time Frame: 6 weeks]
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Waist Circumference (cm)
[Time Frame: 6 weeks]
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Hip Circumference (cm)
[Time Frame: 6 weeks]
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Secondary ID(s)
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CT-92-5581
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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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