Role of Oral Activated Charcoal in reducing Blood cholesterol levels

Effect of Oral Activated Charcoal on Hyperlipidemic Individuals

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/08/015298

Enrollment

Registered

2018-08-13

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Oral Activated Charcoal Incorporated Product (Buttermilk): Participant would be kept on Oral Activated Charcoal Incorporated Product (Buttermilk) for 2 and a half months For 0-4 weeks w

Eligibility

Inclusion criteria

Inclusion criteria: INCLUSION: Patients whose Total cholesterol level is 200-300mg/dl would be recruited between the age group of 35 to 65 years including both males and females who are willing to participate.

Exclusion criteria

Exclusion criteria: EXCLUSION: Age group below 35 years - 65 years above,Pregnant and lactating women and with any other comorbid conditions.Patients that are immuno compromised suffering from terminal illness like HIV, Cancer or those who are under medical treatment.

Design outcomes

Primary

Measure	Time frame
To evaluate the effectiveness of accepted activated charcoal product on lipid profile.Timepoint: 3 times (Pre intervention,end of 4 weeks and 8 weeks)	—

Secondary

Measure	Time frame
â?¢ To evaluate the effectiveness of accepted Activated Charcoal product on lipid profile and anthropometric measurements - Height, weight, Hip Circumference, Waist circumference, waist to hip ratio, MUAC, Skin fold thickness (3 sights - chest, abdomen, thigh for men and triceps, suprailliac, thigh for women) of Hyperlipidemic individuals. Timepoint: 3 times (Pre intervention,end of 4 weeks and 8 weeks);To study the variation in the lipid profile and anthropometric measurements during the 2 weeks wash out period.Timepoint: Only once and at end of 10 weeks of study period.	—

Measure

Time frame

â?¢ To evaluate the effectiveness of accepted Activated Charcoal product on lipid profile and anthropometric measurements - Height, weight, Hip Circumference, Waist circumference, waist to hip ratio, MUAC, Skin fold thickness (3 sights - chest, abdomen, thigh for men and triceps, suprailliac, thigh for women) of Hyperlipidemic individuals. Timepoint: 3 times (Pre intervention,end of 4 weeks and 8 weeks);To study the variation in the lipid profile and anthropometric measurements during the 2 weeks wash out period.Timepoint: Only once and at end of 10 weeks of study period.

—

Countries

India

Contacts

Public ContactLaaksha Monica Paul Motru

Welcomgroup Graduate School of Hotel Administration

pallavi.wgsha@manipal.edu9591273054

Outcome results