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Role of GastriCare in Digestive wellbeing

A Clinical study to evaluate the safety and efficacy of GastriCare in individuals with Functional Dyspepsia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/04/013249
Enrollment
60
Registered
2018-04-13
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: null- Subjects who have clinical symptoms of dyspepsia, upper abdominal pain, heart burn, bloating, indigestion, flatulence, abdominal distension, belching and fullness after meal

Interventions

Intervention1: GastriCare A: 1 capsule of GastriCare A thrice daily Control Intervention1: GastriCare B: 1 capsule of GastriCare B thrice daily

Sponsors

The Himalaya Drug Company
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Subjects of both sexes in the age group of 18 - 60 years, with gastric problems. 2 Subjects who have clinical symptoms of dyspepsia, upper abdominal pain, heart burn, bloating, indigestion, flatulence, abdominal distension, belching and fullness after meal. 3 Subjects willing to give written informed consent. 4 Subjects who have not participated in similar kind of study in last 4 weeks.

Exclusion criteria

Exclusion criteria: 1 Subjects with established hypertension, renal, hepatic or cardiac failure 2 Endocrine disorders 3 Use of prescription medication to treat gastric problems 4 Pregnant & lactating women. 5 Not willing to sign informed consent form.

Design outcomes

Primary

MeasureTime frame
Clinical improvement in the overall health as assessed by clinical examination of signs and symptoms such as epigastric discomfort, heartburn, Nausea, vomiting, belching, flatulence, fullness in the stomach, abdominal distension and the points mentioned in questionnaireTimepoint: baseline, 2nd week and 4th week

Secondary

MeasureTime frame
Compliance of the subject to the drug treatment and the adverse effects will be notedTimepoint: baseline and 4th week

Countries

India

Contacts

Public ContactDr Bindumathi PL MBBS MD

Sapthagiri Institute of Medical Sciences and Research Centre

drbinduraghu@gmail.com080-28393392

Outcome results

None listed

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