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Effect of Topical use of Chamomile oil and Dill oil on Abdominal Obesity

Evaluation of the Effect of Topical use of Chamomile oil and Dill oil on Abdominal Obesity and Comparison with Placebo Group_ A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230902059321N1
Enrollment
60
Registered
2023-10-18
Start date
2022-05-22
Completion date
Unknown
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity. Obesity and other hyperalimentation

Interventions

Intervention 1: Intervention group: In the intervention group for 6 weeks, a combination of chamomile oil and dill oil once a day in the amount of 2 cc per square meter (in such a way that the entire

Sponsors

Research Institute for Islamic and Complementary Medicine (RICM)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: Women between 25 and 55 years Necessary cooperation in taking medicine Women suffering from abdominal obesity Waist circumference greater than 80 cm The possibility of following up patients Fill out a consent form by patients Not pregnant

Exclusion criteria

Exclusion criteria: Not using another topical drug that interferes with the effect of the studied drug Use other weight loss methods Medical condition that prohibits aerobic exercise Patients who do professional sports activities Patients on a weight loss diet History of allergic reaction to topical use of Chamomile oil and Dill oil The presence of an active skin lesion in the study area Women who intend to become pregnant during the treatment period Pregnant women Patient dissatisfaction Hypothyroidism and uncontrolled diabetes mellitus History of using steroid drugs in the last three months

Design outcomes

Primary

MeasureTime frame
Abdominal circumference size. Timepoint: At the beginning of the intervention, then every three weeks until the end of the intervention. Method of measurement: Tape measure.;Abdominal subcutaneous fat thickness in three areas: the thickness of the horizontal skin fold at 3 cm from the navel and 1 cm below it on the right side, the thickness of the skin fold above the navel at the midpoint of the line between the breast and navel junction, the thickness of the left supra iliac skin fold above the iliac crest. In the left midaxillary line. Timepoint: At the beginning of the intervention, then every three weeks until the end of the intervention. Method of measurement: Skinfold Caliper.

Secondary

MeasureTime frame
Body weight. Timepoint: At the beginning of the study and then every three weeks until the end of the study. Method of measurement: Digital weight scale.;Body Mass Index. Timepoint: At the beginning of the study and then every three weeks until the end of the study. Method of measurement: Dividing people's weight (in kilograms) by the square of height (height times height in meters).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Bashiri

Iran University of Medical Sciences

MaryamBashiri18@tahoo.com00 98 55580388

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026