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Efficacy and Safety Study of TroxipTM In the Management of Acid Peptic Disorders

Post Marketing Surveillance (PMS) STUDY ON THE TOLERABILITY AND EFFICACY OF troxip tm (TROXIPIDE 100 mg) in the Management of patients with Acid Peptic Disorders in India.

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2012/11/003133
Enrollment
1500
Registered
2012-11-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K30- Functional dyspepsia Health Condition 2: K25- Gastric ulcer Health Condition 3: K297- Gastritis, unspecified Health Condition 4: K21- Gastro-esophageal reflux disease

Interventions

Intervention1: Troxip: Troxipide 100 mg orally once a day for 28 days Control Intervention1: Not Applicable: Not Applicable

Sponsors

Zuventus Healthcare Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male and Female adult patients. 2. Patients need to be prescribed TroxipTM in order to be enrolled in the surveillance program. 3. Patients of acid-peptic disorders. (Acid peptic disorders are defined as the diseases of either acute or chronic occurrence in the oesophagus, stomach or duodenum. These anatomical gastro-intestinal organs are affected due to the excess acid secretion, which on symptomatic presentation as pain and discomfort by the patients are classified as acid peptic disease). 4. Any other patient to be prescribed TroxipTM as per prescribing information or as per prescribing physicianâ??s discretion.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Safety and TolerabilityTimepoint: for 28 days

Secondary

MeasureTime frame
EfficacyTimepoint: 28 days;patient complianceTimepoint: 28 days

Countries

India

Contacts

Public ContactDr Bhupesh Dewan

Zuventus Healthcare Ltd

bhupesh.dewan@zuventus.com

Outcome results

None listed

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