A clinical study of Appelite Syrup for the treatment of Indigestion, Loss of Appetite, and Acidity.
- Conditions
- Health Condition 1: R630- AnorexiaHealth Condition 2: K30- Functional dyspepsia
- Registration Number
- CTRI/2024/05/067778
- Lead Sponsor
- Healing Hands & Herbs Pvt. Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Patients aged above 18 years of age. 2.Patient with a diagnosis of Dyspepsia (indigestion) or loss of appetite or acidity. 3.Patient or Parent or legal guardian willing to give a written informed consent or parental consent or assent form. 4.Able to or Willing to strictly adhere to the investigator’s prescription.
1.Individuals were excluded if they had taken any medications that might interfere with the action of the study medications prior to the start of the study or during the study.
2.Patients with a medical history and diagnosis of Diabetes were excluded from the study.
3.Female subjects who are pregnant or lactating or planning to become pregnant during the study period. Females who are not ready to use acceptable contraceptive methods during the course
of study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Percentage of Participants with Overall Response. <br/ ><br>2.Evaluate the changes in Dyspepsia (indigestion), Loss of appetite, and RDQ Score.Timepoint: Up to 5 Weeks
- Secondary Outcome Measures
Name Time Method 1.Number of Participants with Treatment-Related Treatment-Emergent Adverse Events (TEAEs). <br/ ><br>2.Safety evaluation of Appelite syrup. <br/ ><br>3.Incidence of adverse events (AEs).Timepoint: Up to 5 Weeks