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Treatment of Gastro-esophageal Reflux Disease in Victims of Mustard Gas Exposure with Chronic Cough

Effects of Anti-reflux Therapy with Omeprazole on Gastrointestinal and Respiratory Symptoms in Victims of Mustard Gas Exposure with Chronic Cough

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012072510398N1
Enrollment
60
Registered
2012-08-17
Start date
2008-01-01
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

Gastro-oesophageal reflux disease. Gastro-oesophageal reflux disease

Interventions

Intervention 1: Omeprazole (20 mg twice daily) for four months followed by one month washout and four months of placebo. Intervention 2: Reverse treatment: Placebo twice daily for four months, then on
Treatment - Drugs
Placebo
Omeprazole (20 mg twice daily) for four months followed by one month washout and four months of placebo
Reverse treatment: Placebo twice daily for four months, then one month washout period, then omeprazole 20 mg twice daily for four months

Sponsors

Chemical Injuries Research Center, Baqiyatallah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Male; Chemical warfare victim; Having a history of exposure to mustard gas; Having symptoms of chronic cough (more than 3 weeks); Having symptoms of GERD; Willing to participate Exclusion criteria: Current smokers; Having previous history of smoking; Being under recent anti-reflux therapy; Contraindication for using omeprazole

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
GERD Symptoms. Timepoint: Before and After the Trial. Method of measurement: Questionnaire.;Cough Symptoms. Timepoint: Every one month. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Quality of Life. Timepoint: Before and After the Trial. Method of measurement: Questionnaire.;Pulmonary Function. Timepoint: Before and After the Trial. Method of measurement: Spirometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammad Talaei

Isfahan University of Medical Sciences and Poursina Hakim Research Institute

mtalaei@gmail.com+98 31 1668 0168

Outcome results

None listed

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