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The effect of ????Duloxetine with lansoprazole on the treatment of Gastroesophageal reflux disease

A Comparison between lansoprazole with placebo and lansoprazole with duloxetine regimens on symptom and quality of life improvement in patients with Gastroesophageal reflux diseases

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141201020178N6
Enrollment
54
Registered
2018-02-04
Start date
2017-12-03
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

gastroesophageal reflux. Gastro-esophageal reflux disease

Interventions

Intervention 1: Intervention group: Tablet Lansoprazole 30 mg daily with Capsule Duloxetine 30 mg daily(Abidi company). Intervention 2: Control group: Tablet Lansoprazole 30 mg daily with Capsule plac

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: age between 18-65 Typical symptoms of Gastro -esophageal reflux disease (heartburn, regurgitation)and/ or endoscopic findings of Gastroesophageal reflux disease

Exclusion criteria

Exclusion criteria: Use of recent or previous anti-depressants and anti- anxiety drugs A history of allergy to any of the medications History of alcohol consumption Atypical symptoms of Gastro esophageal reflux disease Previous history of anxiety or depression History of opium use History of upper gastrointestinal disorders(Dyspepsia and/or Peptic ulcer disease) History of cardiac , pulmonary , musculoskeletal disease and any malignancy. History of medications such as: Sildenafil, calcium channel blocker, methylxanthine, nitrate and beta-agonist Age under 18 years Age older than sixty-five

Design outcomes

Primary

MeasureTime frame
Quality and symptoms of patients with gastroesophageal reflux Disease. Timepoint: Before starting the intervention and 4 weeks later. Method of measurement: Patient Assessment of gastroesophageal re flux Quality of life and symptom Questionnaires.

Secondary

MeasureTime frame
Adverse effect of medications. Timepoint: 2 and 4 weeks after starting the intervention. Method of measurement: Data gathering sheet of patients.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarjan Mokhtare

Iran University of Medical Sciences

marjanmokhtare@yahoo.com+98 21 6655 4790

Outcome results

None listed

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