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A clinical study of Appelite Syrup for the treatment of Indigestion, Loss of Appetite, and Acidity.

A prospective, open label, single centre study for evaluation of efficacy and safety of Appelite Syrup in the management of Dyspepsia (Indigestion),Loss of Appetite And Acidity - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067778
Enrollment
550
Registered
2024-05-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: R630- Anorexia Health Condition 2: K30- Functional dyspepsia

Interventions

None listed

Sponsors

Healing Hands & Herbs Pvt. Ltd.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

Exclusion criteria: 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.

Design outcomes

Primary

MeasureTime frame
1.Percentage of Participants with Overall Response. 2.Evaluate the changes in Dyspepsia (indigestion), Loss of appetite, and RDQ Score.Timepoint: Up to 5 Weeks

Secondary

MeasureTime frame
1.Number of Participants with Treatment-Related Treatment-Emergent Adverse Events (TEAEs). 2.Safety evaluation of Appelite syrup. 3.Incidence of adverse events (AEs).Timepoint: Up to 5 Weeks

Countries

India

Contacts

Public ContactDr Gajanan Bhagwat

Healing Hands Clinic Pvt. Ltd.

drashwinporwal@healinghandsclinic.co.in9822347770

Outcome results

None listed

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