Effect of Herbal Compositions on Body Weight, Body Composition and Metabolic Health in Overweight Subjects

ApexCPG LLC

Status: Not yet enrolling

Conditions: Healthy Participants

Treatments: Other: Placebo; Dietary Supplement: CL24212; Dietary Supplement: CL19183

Study type: Interventional

Funder types: Industry

Identifiers

NCT07083947

APX/OW/CL24212/25

Details and patient eligibility

About

The Purpose of the study is to evaluate the efficacy of herbal composition CL19183 and CL24212 on body weight, body composition and metabolic health in overweight subjects.

Full description

A total of 150 male and female subjects aged between 25 and 55 years will be included in the study. Assessment of inclusion and exclusion criteria will be done based on clinical and laboratory investigations. The eligible subjects will be randomized as per the computer-generated randomization list. The subjects will be assigned to either CL19183:450 mg or CL24212:300 mg or Placebo arm at 1:1:1 ratio. The subjects will be instructed to take one capsule daily in the morning after breakfast for 16 weeks. Apart from primary and secondary outcomes, the study will also record the vital signs and adverse events to evaluate the herbal composition safety and tolerability. The safety assessment of the CL19183 and CL24212 will also include routine laboratory investigations on blood, urine and clinical chemistry at screening and the final visit of the intervention

Enrollment: 150 estimated patients

Sex: All

Ages: 22 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 1. Healthy male and female subjects aged between 25-55 years with body mass index (BMI) of 25-29.9 kg/m2.

  2. Subjects with sedentary lifestyle, no regular athletic or sports activities. 3. Subjects willing to participate in walking-exercise (5 days a week, 30 min per day) over study duration.

  3. Subjects with normal thyroid hormone profile. 5. Subjects agreed to consume recommended standard diet. 6. Subjects who are willing to abstain from alcohol, coffee, tea, cola, energy drinks & chocolate for at least 24 hrs. prior to visits and final visit.

  4. Subjects who are non-smokers. 8. Subject agrees to maintain diet tracker. 9. Subject considered generally healthy as per health history and routine clinical investigations during screening.

  5. Female subjects of childbearing potential must be using a medically acceptable form of birth control for at least 1 month prior to screening (3 months on oral contraceptives), e.g., oral or patch contraceptives, intrauterine device, Depo-Provera®, or double-barrier and have a negative pregnancy test at the screening visit.

  6. Ability to understand the risks/benefits of the protocol and willing to sign the written informed consent.

Exclusion criteria

• 1. Subjects who were taking medications which affect the metabolic rate (e.g. antidepressants, beta-blockers, hormones, etc.).

  2. Subjects on weight loss practices, usage of weight reduction supplements/nutrition products will be excluded.

  3. Subjects underwent treatment for COVID 19 within last 3 months or tested positive during the study will be excluded.

  4. Subjects participated in any weight loss programs within 3 months. 5. Subjects who are diabetic and/or hypertensive. 6. Evidence or history of hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, neurologic diseases, malignancies.

  5. Subjects taking medications for or suffering from a medical condition that could impact results related to metabolism (e.g., thyroid disorders, diabetes, mental disorders such as anxiety or depression, heart disease, arthritis, cancer).

  6. Subjects with HIV Positive. 9. Female subjects, who are pregnant, breast feeding or planning to become pregnant during the study.

  7. Subjects having history of psychiatric disorder that may impair the ability of subjects to provide written informed consent.

  8. Any other condition that, in the opinion of the investigator, would adversely affect the subject's ability to complete the study or its measures.

  9. Use of nutritional supplements (e.g., creatine, protein drinks, amino acids, or vitamins) or ergogenic aids and caffeinated and not caffeinated thermogenics within 30 days prior to the study.

  10. Subjects who are participated or currently participating in another clinical trial within 30 days prior to screening.

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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150 participants in 3 patient groups, including a placebo group

Placebo

Placebo Comparator group

Description:

One capsule taken orally each morning after breakfast with water for 16 weeks

Treatment:

Other: Placebo

CL19183

Experimental group

Description:

One capsule taken orally each morning after breakfast with water for 16 weeks

Treatment:

Dietary Supplement: CL19183

CL24212

Experimental group

Description:

One capsule taken orally each morning after breakfast with water for 16 weeks

Treatment:

Dietary Supplement: CL24212