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Pistacia atlantica Oleoresin of preparation on weight loss

Phase 3
Recruiting
Conditions
overweight and obesity.
Obesity, unspecified
E66.9
Registration Number
IRCT20221022056262N1
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
60
Inclusion Criteria

Women with mild to moderate initial overweight and obesity(BMI 25-39.9)

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The amount of weight change (body mass index) in overweight and obese women. Timepoint: Measurement of body mass index before the intervention, 30, 60, and 90 days after the start of the intervention. Method of measurement: Digital weighing machine.
Secondary Outcome Measures
NameTimeMethod
Measurement of the size of the abdomen. Timepoint: At the beginning of the study (before the start of the intervention), 30, 60, and 90 days after the start of intervention. Method of measurement: Measuring meter.;Blood cholesterol, triglycerides, LDL and HDL levels. Timepoint: At the beginning of the study (before the start of the intervention) and 60 days after the start of the intervention. Method of measurement: blood test.;Measure the size of the hip circumference. Timepoint: At the beginning of the study (before the start of the intervention), 30, 60, and 90 days after the start of intervention. Method of measurement: Measuring meter.;Measurement of the ratio of the size of the abdominal circumference to the size of the hip circumference. Timepoint: At the beginning of the study (before the start of the intervention), 30, 60, and 90 days after the start of intervention. Method of measurement: Measuring meter.
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