Trial ID: | L0836 |
Source ID: | IRCT2015120925447N1
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Associated Drug: |
Zaharia
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Title: |
The effect of Zataria multiflora Boiss in the treatment of non alcoholic fatty liver disease
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Acronym: |
--
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Status: |
Not Recruiting
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Study Results: |
No Results Available
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Results: |
--
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Conditions: |
Non alcoholic fatty liver. <br>Non alcoholic fatty liver disease;K 76.0;Non alcoholic fatty liver disease
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Interventions: |
Intervention 1: Intervention group : 700 mg (two 350 mg cap ) Shirazi thyme powder bid for 90 days. Intervention 2: Control group : 700 mg (two cap 350 mg ) wheat powder bid for 90 days.;Treatment - Drugs;Placebo;Intervention group : 700 mg (two 350 mg ca
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Outcome Measures: |
Alaninaminotransferase. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.;Grade of fatty liver. Timepoint: Before intervention and three months after intervention. Method of measurement: Ultrasonography.Blood pressure. Timepoint: Before intervention and three months after intervention. Method of measurement: By manometer according to mmHg.;Fasting blood sugar. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.;Aspartateaminotransferase. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.;Body mass index. Timepoint: Before intervention and three months after intervention. Method of measurement: Scale and measuring tape.;Waist circumference. Timepoint: Before intervention and three months after intervention. Method of measurement: By measuring tape.;Hip circumference. Timepoint: Before intervention and three months after intervention. Method of measurement: By measuring tape.;Insulin. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.;Lipid profile. Timepoint: Before intervention and three months after intervention. Method of measurement: Blood sampling.
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Sponsor/Collaborators: |
Vice chancellor for research, Shiraz University of Medical Sciences
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Gender: |
All
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Age: |
20 years65 years
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Phases: |
Not applicable
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Enrollment: |
90
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Study Type: |
interventional
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Study Designs: |
Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
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Start Date: |
16/10/2016
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Completion Date: |
--
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Results First Posted: |
--
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Last Update Posted: |
22 February 2018
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Locations: |
Iran (Islamic Republic of);Iran (Islamic Republic of)
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URL: |
http://en.irct.ir/trial/21282
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