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Comparison of two types of standard Three drug regimen treatments in dyspepsia due to H. pylori infection.

To compare the efficacy and safety of triple regimens Pantoperazole, Amoxicillin, Clarithromycin versus Pantoperazole, Metronidazole, Clarithromycin for Helicobacter Pylori Eradication in Dyspepsia patients; A Randomised controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/024057
Enrollment
60
Registered
2020-03-19
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: K269- Duodenal ulcer, unspecified as acute or chronic, without hemorrhage or perforation Health Condition 2: K30- Functional dyspepsia Health Condition 3: K259- Gastric ulcer, unspecified as acute or chronic, without hemorrhage or perforation Health Condition 4: K299- Gastroduodenitis, unspecified Health Condition 5: K279- Peptic ulcer, site unspecified, unspecified as acute or chronic, without hemorrhage or perforation

Interventions

Intervention1: Triple Drug Regimen PAC: Tab Pantoperazole 40 mg BD half hour before meals per oral x 14 days, Cap Amoxicillin 1gm (500mg, 2 capsules) BD per oral X 14 Days, Tab Clarithromycin 500mg BD

Sponsors

DR Rajendra Prasad Government Medical College Kangra at Tanda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Dyspepsia patients (ulcer or non-ulcer) with H. pylori positivity on gastric biopsy.

Exclusion criteria

Exclusion criteria: 1) Patients not willing to give written informed consent. 2) Pregnant females. 3) Lactating females. 4) Active alcohol users. 5) Patients allergic or with known contraindications to any of study drugs. 6) Patients who have already taken either of the above mentioned H. pylori eradication regimens.

Design outcomes

Primary

MeasureTime frame
Eradication of Helicobacter pylori as indicated by stool antigenTimepoint: 1.5 months after initiation of treatment.

Secondary

MeasureTime frame
To evaluate the safety profile of two triple drug regimenTimepoint: From initiation of treatment to 1.5 months after initiation of treatment.

Countries

India

Contacts

Public ContactDr Dinesh Kansal

DR. Rajendra Prasad Government Medical College Kangra at Tanda

ajay.igmc20044@gmail.com9418138661

Outcome results

None listed

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