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Comparing Omeprazole With Fluoxetine for Treatment of Non Erosive Reflux Disease and Its Subgroups: a Double-blind Placebo-controlled Clinical Trial

Primary Purpose

Non-erosive Reflux Disease

Status
Completed
Phase
Phase 2
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Fluoxetine
Omeprazole
placebo
Omeprazole
Fluoxetine
placebo
Sponsored by
Tehran University of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non-erosive Reflux Disease focused on measuring non-erosive reflux disease, heartburn, functional, Antidepressive Agents, Second-Generation, Proton Pump Inhibitors

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age above 18 and below 60 years old
  • experiencing heartburn during last 6 months before inclusion
  • experiencing heartburn during at least 4 of 7 days before inclusion
  • presence of normal mucosa in upper gastrointestinal(GI) endoscopy which has been documented during 7 days before inclusion provided that the patient has not administered any PPI during last 30 days before inclusion

Exclusion Criteria:

  • inability to undergone upper GI endoscopy or PH monitoring
  • presence of barret's esophagus or erosive esophagitis in upper GI endoscopy
  • presence of active peptic ulcer disease or any disease which affects the absorption of drugs such as inflammatory bowel disease
  • past history of esophageal or gastric surgery
  • esophageal stricture which needs dilation
  • administration of proton pomp inhibitors during 30 days before inclusion to the study
  • administration of H2 blockers, anticholinergics, sucralfate and pro-kinetics during the assessments for eligibility and also during the study
  • long time administration of non-steroidal anti-inflammatory drugs (NSAIDs)
  • administration of neuroleptic or antidepressant drugs during 30 days before inclusion to the study
  • known allergy to PPIs or SSRIs
  • presence of significant systemic disease such as scleroderma , diabet mellitus , peripheral and autonomic neuropathies and ...
  • pregnancy for females
  • presence of known psychiatric disorder such as depression , panic disorder or drug addiction according to the DSM-IV criteria

Sites / Locations

  • Gasterointestinal endoscopy ward, Amir Alam hospital, Tehran university of medical sciences

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Active Comparator

Placebo Comparator

Active Comparator

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

pH positive-omeprazole

pH positive-placebo

pH positive-fluoxetine

pH negative-omeprazole

pH negative-fluoxetine

pH negative-placebo

Arm Description

Outcomes

Primary Outcome Measures

investigator-reported symptom severity
symptom severity at beginning and 6 weeks after the study ,assessed by the standard questionnaire

Secondary Outcome Measures

patient-reported symptom severity
symptom severity reported by the patient in daily diary
heartburn-free days
percentage of 24-h heartburn-free days (days with neither daytime nor nighttime heartburn) during treatment assessed by daily diary

Full Information

First Posted
December 21, 2010
Last Updated
March 5, 2012
Sponsor
Tehran University of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT01269788
Brief Title
Comparing Omeprazole With Fluoxetine for Treatment of Non Erosive Reflux Disease and Its Subgroups: a Double-blind Placebo-controlled Clinical Trial
Official Title
Comparing Omeprazole With Fluoxetine for Treatment of Non Erosive Reflux Disease and Its Subgroups: a Double-blind Placebo-controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
August 2010 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
August 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tehran University of Medical Sciences

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Gastro-esophageal reflux disease (GERD) is highly prevalent, affecting up to 20% of the adult population in North America. Up to 70% of GERD patients have non-erosive reflux disease (NERD), a term used to describe symptoms suggestive of GERD in patients with no endoscopic evidence of erosive esophagitis. NERD represents a heterogeneous group of patients whom are sub classified according to 24 hours-PH monitoring results and also symptom-acid association analysis(Symptom Index,SI). Treatment of NERD can be a challenge for clinicians. According to the many studies , the pooled rate for symptomatic response after a period of proton pomp inhibitor(PPIs)therapy as the most frequently used drug, in NERD patients is lower than for erosive esophagitis patients. It is also shown that acid exposure is much lower in NERD patients than those with erosive esophagitis and NERD patients are less likely to exhibit a strong association between heartburn symptoms and acid reflux events than patients with erosive oesophagitis. Furthermore, beside the high economic burden, there are concerns about the adverse effects of long time administration of PPIs. Several hypothesis has been proposed to describe low response rate of NERD patients to PPIs. One of the most acceptable theories is that patients with anxiety or depression and psychological problems are at an increased risk of developing reflux symptoms. On the other hand, pain modulators such as sertraline, a selective serotonin reuptake inhibitor(SSRI), and other antidepressants have been shown to improve symptoms in patients with functional gastrointestinal disorders like non cardiac chest pain. According to the above-mentioned tips, the investigators hypothesize that antidepressants like fluoxetine, as an SSRI, may have beneficial effects in improving symptoms of NERD patients. The purpose of this study is to compare the effect of omeprazole with fluoxetine and placebo for treatment of NERD patients and its subgroups who all experience reflux symptoms and have normal endoscopic findings.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-erosive Reflux Disease
Keywords
non-erosive reflux disease, heartburn, functional, Antidepressive Agents, Second-Generation, Proton Pump Inhibitors

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
144 (Actual)

8. Arms, Groups, and Interventions

Arm Title
pH positive-omeprazole
Arm Type
Active Comparator
Arm Title
pH positive-placebo
Arm Type
Placebo Comparator
Arm Title
pH positive-fluoxetine
Arm Type
Active Comparator
Arm Title
pH negative-omeprazole
Arm Type
Active Comparator
Arm Title
pH negative-fluoxetine
Arm Type
Active Comparator
Arm Title
pH negative-placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Fluoxetine
Intervention Description
20 mg , oral , daily 30 mins before breakfast, for 6 weeks
Intervention Type
Drug
Intervention Name(s)
Omeprazole
Intervention Description
20 mg , oral , daily 30 mins before breakfast, for 6 weeks
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
oral , daily 30 mins before breakfast, for 6 weeks
Intervention Type
Drug
Intervention Name(s)
Omeprazole
Intervention Description
20 mg , oral , daily 30 mins before breakfast, for 6 weeks
Intervention Type
Drug
Intervention Name(s)
Fluoxetine
Intervention Description
20 mg , oral , daily 30 mins before breakfast, for 6 weeks
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
oral , daily 30 mins before breakfast, for 6 weeks
Primary Outcome Measure Information:
Title
investigator-reported symptom severity
Description
symptom severity at beginning and 6 weeks after the study ,assessed by the standard questionnaire
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
patient-reported symptom severity
Description
symptom severity reported by the patient in daily diary
Time Frame
6 weeks
Title
heartburn-free days
Description
percentage of 24-h heartburn-free days (days with neither daytime nor nighttime heartburn) during treatment assessed by daily diary
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age above 18 and below 60 years old experiencing heartburn during last 6 months before inclusion experiencing heartburn during at least 4 of 7 days before inclusion presence of normal mucosa in upper gastrointestinal(GI) endoscopy which has been documented during 7 days before inclusion provided that the patient has not administered any PPI during last 30 days before inclusion Exclusion Criteria: inability to undergone upper GI endoscopy or PH monitoring presence of barret's esophagus or erosive esophagitis in upper GI endoscopy presence of active peptic ulcer disease or any disease which affects the absorption of drugs such as inflammatory bowel disease past history of esophageal or gastric surgery esophageal stricture which needs dilation administration of proton pomp inhibitors during 30 days before inclusion to the study administration of H2 blockers, anticholinergics, sucralfate and pro-kinetics during the assessments for eligibility and also during the study long time administration of non-steroidal anti-inflammatory drugs (NSAIDs) administration of neuroleptic or antidepressant drugs during 30 days before inclusion to the study known allergy to PPIs or SSRIs presence of significant systemic disease such as scleroderma , diabet mellitus , peripheral and autonomic neuropathies and ... pregnancy for females presence of known psychiatric disorder such as depression , panic disorder or drug addiction according to the DSM-IV criteria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Seyed Amir Mirbagheri, MD
Organizational Affiliation
Department of Internal Medicine, Faculty of medicine, Tehran university of medical sciences
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mohammad Reza Ostovaneh, MD,MPH
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Arash Etemadi, MD, PhD
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yasin Farrokhi Khajeh Pasha, MD, MPH
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Behtash Saeidi, MD
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kaveh Hajifathalian, MD
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Akbar Fotouhi, MD, PhD
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Seyed Mahmoud Eshagh hosseini, MD
Organizational Affiliation
Tehran University of Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gasterointestinal endoscopy ward, Amir Alam hospital, Tehran university of medical sciences
City
Tehran
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

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Comparing Omeprazole With Fluoxetine for Treatment of Non Erosive Reflux Disease and Its Subgroups: a Double-blind Placebo-controlled Clinical Trial

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