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Clinical Trial on Kapiva Weight Wise Foods Get Slim Plus Juice

A parallel arm clinical trial validating safety and efficacy of Kapiva Weight Wise Foods Get Slim Plus Juice for weight management and to measure changes in anthropometric parameters and QOL - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050908
Enrollment
30
Registered
2023-03-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: E669- Obesity, unspecified

Interventions

Intervention1: Kapiva Weight Wise Foods Get Slim Plus Juice: 30 ml Kapiva Weight Wise Foods Get Slim Plus Juice should be consumed twice a day, one hour before meals, in the afternoon and evening mixe

Sponsors

Adret Retail Pvt Ltd (Kapiva Ayurveda)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Male/female patients aged between 20-45 years (both inclusive) with BMI between 25-35 kg/m2;2.Patient with or without hypothyroidism. Patients with hypothyroidism on medication should be stable and have a normal TSH level;3.Patients with or without comorbidities, if comorbidity exists should be on stable prescription and with following criteria- Hypertension (Less than or equal to 140/90 mmHg on prescription), Type 2 DM (HbA1C less than or equal to 7.5 on prescription);4.Willing to provide consent; 5.Willing for follow up.

Exclusion criteria

Exclusion criteria: 1.Patients with any acute illness requiring immediate medical care. 2.Patients with PCOS, PCOD, infertility disorder or any other hormonal disorder. 3.Patients with Type I DM/Complicated cardiovascular diseases / HbA1C greater than or equal to 7.5/ history of TIA, cerebrovascular accident, stroke or any revascularization. 4.Known patients of hepatic failure/renal impairment. 5.Pregnant, breastfeeding or planning to become pregnant during the study. 6.Any other condition which proves the patient unfit for the study participation.

Design outcomes

Primary

MeasureTime frame
1.Changes in body weight and body mass index (BMI) on screening, visit 2, visit 3, visit 4, visit 5, visit 6, visit 7. 2.Changes in anthropometric parameters such as waist/hip ratio, mid upper arm circumference, body fat %, visceral fat level % on screening, visit 3, visit 5 and visit 7. 3.Changes in the Quality of life of patients by IWQOL-Lite score (The Impact of Weight on Quality-of-Life Questionnaire) in social and emotional aspect on screening, visit 3, visit 5, visit 7. 4.Changes in the number of high to moderate energy events from energy audit diary on screening, visit 3, visit 5, visit 7.Timepoint: Screening visit ,Visit 2,Visit 3,Visit 4,Visit 5,Visit 6,Visit 7

Secondary

MeasureTime frame
1.Changes in digestive behavior (Bloating, Heartburn, Flatulence, Constipation, Post Prandial Fullness, etc.) in patients on screening, visit 2, visit 3, visit 4, visit 5, visit 6, visit 7. 2.Changes in lipid profile on screening, and visit 7. 3.Changes in general complaints like profuse sweating, irregular thirst, dyspnea, and craving on 0-10 VAS score screening, visit 2, visit 3, visit 4, visit 5, visit 6, visit 7.Timepoint: Screening visit ,Visit 2,Visit 3,Visit 4,Visit 5,Visit 6,Visit 7

Countries

India

Contacts

Public ContactDr Kriti Soni

Adret Retail Pvt Ltd (Kapiva Ayurveda)

kriti.soni@kapiva.in9871018383

Outcome results

None listed

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