A scientific study to check the effect of a tonic in hunger lost patients.
- Conditions
- Health Condition 1: R630- Anorexia
- Registration Number
- CTRI/2019/07/020268
- Lead Sponsor
- Dr Nagaraj S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
1.Adult male or female patients aged 18 to 55 years of age.
2.Patients with a history of loss of appetite and a CNAQ appetite score of <28 due to acute or chronic illness.
3.Participants should have the ability to understand the requirements of the study.
4.Participants willing to abide by the study restrictions and return for the required assessments.
5.Participants willing to sign informed consent document.
1.Patients less than 18 years or older than 55 years of age.
2.Pregnant and lactating women
3.Patients with or currently taking any antihistaminic or ayurvedic tonics for appetite loss during and 7 days before the study.
4.Patients with known history of hypersensitivity to the study drug used for therapy of appetite loss
5.Patients with a known condition that may interfere with the study drugâ??s absorption or metabolism at physicianâ??s discretion.
Study & Design
- Study Type
- PMS
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the effectiveness of an appetite stimulating tonic containing multi-vitamins, lysine and zinc in patients with loss of appetite.Timepoint: 7 Days
- Secondary Outcome Measures
Name Time Method â?¢To evaluate the effectiveness of an appetite stimulating tonic containing multi-vitamins, lysine and zinc in patients with loss of appetite. <br/ ><br>â?¢To assess the change in Council on Nutrition Appetite Questionnaire (CNAQ) appetite. <br/ ><br>â?¢To assess the safety of an appetite stimulating tonic containing multi-vitamins, lysine and zinc in patients with loss of appetite.Timepoint: 14 Days