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The effect of Clidinium c on peptic ulcer treatment

The effect of clidinium c with triple therapy in comparison with standard triple therapy for helicobacter pylori eradication in peptic ulcer patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013041112977N1
Enrollment
66
Registered
2013-07-29
Start date
2013-03-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

peptic ulcer. gastroduodenal ulcer NOS peptic ulcer NOS

Interventions

Intervention 1: Intervention 1 : Capsule Omeprazol 40 miligram(mg) (Osveh Pharmaceutical Company) , Tablet (tab)clarithromycine 1 gram(gr) (Chemidarou Pharmaceutical Company) and capsule amoxicilline
Treatment - Drugs
Intervention 2 : Capsule Omeprazol 40 miligram(mg) (Osveh Pharmaceutical Company) , Tablet (tab)clarithromycine 1 gram(gr) (Chemidarou Pharmaceutical Company) and capsule amoxicilline 2 gr (Kosar Phar
Intervention 1 : Capsule Omeprazol 40 miligram(mg) (Osveh Pharmaceutical Company) , Tablet (tab)clarithromycine 1 gram(gr) (Chemidarou Pharmaceutical Company) and capsule amoxicilline 2 gr (Kosar Phar

Sponsors

Vice chancellor for research, Golestan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with peptic ulcer in endoscopy and positive rapid urease test for helicobacter pylori (HP) infection are enrolled. Exclusion criteria: Patients that are taking non steroid anti-inflammatory drugs (NSAIDs), proton pump inhibitors (PPIs), bismuth preparations or antibiotics during the last four weeks and with prior HP eradication, glaucoma, prostatic hypertrophy, pregnancy , lactation and intolerable side effects of clidinium-c are excluded.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Helicobacter pylori eradication. Timepoint: Before and 8 weeks after intervention. Method of measurement: Before intervention in antrum sample with rapid urease test and 8 weeks after intervention with urease breathe test.

Secondary

MeasureTime frame
Age. Timepoint: Before intervention. Method of measurement: Year-Birth certificate.;Sex. Timepoint: Before intervention. Method of measurement: Female/male-Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaba Homapour

Golestan University of Medical Sciences

homapoorsaba@yahoo.com+98 17 1442 1653

Outcome results

None listed

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