Poleium Teucrium supplementation ,exercise and chylomicron, HDL and KCL

The effects of Poleium Teucrium supplementation and a course selected exercise on chylomicron, HDL and KCL on military men 20-25 years old

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20171210037809N5

Enrollment

130

Registered

2019-08-04

Start date

2019-06-26

Completion date

Unknown

Last updated

2019-10-07

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

Conditions

There is no illness / the effect of the toner is to be practiced.

Interventions

Intervention 1: Intervention group: Teucrium polium and exercise,The group 1 week before training received 125 mg of Teucrium polium tropic extract every day.The Teucrium polium used by the Irania

Eligibility

Sex/Gender

Male

Age

20 Years to 25 Years

Inclusion criteria

Inclusion criteria: 1.Over the past six months, they have not consumed any supplements or medications It does not exclude any history of common chronic health problems and diseases, such as respiratory, metabolic, cardiovascular, renal and hepatic diseases

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Triglyceride. Timepoint: At the beginning of the study (before the intervention) and after 8 weeks of supplementation and exercise. Method of measurement: Blood collection :changes triglyceride : mg / dl.;HDL. Timepoint: At the beginning of the study (before the intervention) and after 8 weeks. Method of measurement: Blood collection :changes HDL : mg / dl.;LDL. Timepoint: At the beginning of the study (before the intervention) and after 8 weeks. Method of measurement: Blood collection :changes LDL : mg / dl.	—

Measure

Time frame

Triglyceride. Timepoint: At the beginning of the study (before the intervention) and after 8 weeks of supplementation and exercise. Method of measurement: Blood collection :changes triglyceride : mg / dl.;HDL. Timepoint: At the beginning of the study (before the intervention) and after 8 weeks. Method of measurement: Blood collection :changes HDL : mg / dl.;LDL. Timepoint: At the beginning of the study (before the intervention) and after 8 weeks. Method of measurement: Blood collection :changes LDL : mg / dl.

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Countries

Iran (Islamic Republic of)

Contacts

Public Contactehsan roostaii

Islamic Azad University

dastavard96@gmail.com+98 21 3672 5014

Outcome results

None listed

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