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SThe Effects of Melatonin on GERD Symptoms

Primary Purpose

Gastroesophageal Reflux Disease

Status
Unknown status
Phase
Phase 1
Locations
Israel
Study Type
Interventional
Intervention
Melatonin
omeprazole
Placebo
Sponsored by
Rabin Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastroesophageal Reflux Disease

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

INCLUSION CRITERIA:

  • Ages 18-75.
  • Male or female.
  • GERD symptoms at least twice a week for the last three months.
  • Able to read, understand and complete study questionnaires and diary
  • Understand the study procedures and sign written informed consent.
  • Able to comply with all study requirements.

EXCLUSION CRITERIA:

  • Subjects with erosive esophagitis (EE), Barrett's esophagus (BE) and esophageal stricture or adenocarcinoma on upper endoscopy.
  • Subjects with previous upper gastrointestinal surgery.
  • Subjects with clinically significant medical conditions (cardiovascular, respiratory, renal, hepatic, hematologic, endocrine, neurologic and psychiatric); examples as follows: liver cirrhosis, severe COPD, severe renal failure, severe heart failure, active malignancy.
  • Subjects requiring narcotics (morphine, methadone, etc.).
  • Subjects requiring melatonin
  • Subjects with diabetes, scleroderma and neuromuscular disorders.
  • Lactating or pregnant women.
  • Subjects with an unrecognized lifestyle such as shift workers.

Sites / Locations

  • Rabin Medical Center, Beilinson Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Experimental

Arm Label

A

B

C

Arm Description

Melatonin treatment group

Omeprazole 20 mg once a day for 3 months

Placebo once a day for 3 months

Outcomes

Primary Outcome Measures

This study will test the efficacy of melatonin (10 mg once a day) as compared to standard dose PPI (omeprazole 20 mg once a day) and placebo on different subjective and objective parameters of 150 patients with GERD.

Secondary Outcome Measures

To determine the effect of melatonin versus standard-dose PPI versus placebo on frequency and duration of TLESRs.

Full Information

First Posted
November 26, 2007
Last Updated
November 26, 2007
Sponsor
Rabin Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT00564590
Brief Title
SThe Effects of Melatonin on GERD Symptoms
Official Title
The Effects of Melatonin on GERD Symptoms and Esophageal Acid Exposure
Study Type
Interventional

2. Study Status

Record Verification Date
November 2007
Overall Recruitment Status
Unknown status
Study Start Date
October 2008 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Rabin Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
We hypothesize that melatonin as compared to PPI and to placebo, improves GERD symptoms by decreasing esophageal acid exposure and esophageal acid sensitivity in GERD. We hypothesize that melatonin as compared to PPI and to placebo reduce the frequency and duration of transient lower esophageal sphincter relaxations (TLESRs). In addition we hypothesize that melatonin as compared to PPI and to placebo improves quality of life and quality of sleep of GERD patients.
Detailed Description
Background: Gastroesophageal reflux disease (GERD) is a chronic, persistent and common medical problem. The standard of care for GERD includes chronic administration of acid-suppressive drugs. However, clinical failure in GERD is increasingly reported. Aim: To determine the efficacy of treatment with melatonin as compared to standard dose proton pump inhibitor (PPI) as compared to placebo in patients with GERD. Study objectives: [1] To compare the degree of GERD symptoms improvement and esophageal acid sensitivity before and after treatment. [2] To determine the effect of treatment on the % total, upright and supine time pH <4 using 24-hour esophageal pH monitoring. [3] To determine the effect of treatment on frequency and duration of lower esophageal sphincter relaxation. [4] To compare the quality of life and quality of sleep in GERD patients before and after treatment. Methods: This is a randomized, double blind, parallel groups study of 150 patients with GERD. Patients with classic heartburn symptoms (heartburn and/or regurgitation) and normal upper endoscopy from the gastroenterology department at Rabin Medical Center will be enrolled into the study. At baseline, all enrolled patients will have 24-hour esophageal pH monitoring and a modified acid perfusion test to assess the extent of distal esophageal acid exposure and esophageal acid sensitivity, respectively. Patients will be evaluated by a demographics questionnaire, the GERD Symptom Questionnaire, the Quality of Sleep questionnaire and the SF-36. Baseline urinary excretion of the main melatonin metabolite, 6-sulfatoxymelatonin (6SMT) will be assessed in all subjects at baseline. Patients will be randomized to either melatonin or standard dose PPI or placebo over a period of 4 weeks. In addition patients will fill a diary on a daily basis that documents severity and frequency of GERD-related symptoms. Symptom score (frequency x severity) will be calculated for previous 7 days at baseline and at the end of treatment in all groups. After 4 weeks of treatment, patients will undergo a second 24-hour esophageal pH monitoring, a modified acid perfusion test and will complete the GERD Symptom Questionnaire, the Quality of Sleep Questionnaire and the SF-36. Implications: This study will determine if melatonin decreases GERD symptoms, acid esophageal exposure and improves quality of life and sleep in patients with GERD. Furthermore, if there will be a significant clinical response to melatonin it will be possible to add this compound to the treatment armamentum of GERD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Melatonin treatment group
Arm Title
B
Arm Type
Active Comparator
Arm Description
Omeprazole 20 mg once a day for 3 months
Arm Title
C
Arm Type
Experimental
Arm Description
Placebo once a day for 3 months
Intervention Type
Drug
Intervention Name(s)
Melatonin
Intervention Description
4 mg of Melatonin once a day for 3 months
Intervention Type
Other
Intervention Name(s)
omeprazole
Other Intervention Name(s)
Omepradex
Intervention Description
omeprazole 20 mg once a day
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo once a day
Primary Outcome Measure Information:
Title
This study will test the efficacy of melatonin (10 mg once a day) as compared to standard dose PPI (omeprazole 20 mg once a day) and placebo on different subjective and objective parameters of 150 patients with GERD.
Time Frame
3 years
Secondary Outcome Measure Information:
Title
To determine the effect of melatonin versus standard-dose PPI versus placebo on frequency and duration of TLESRs.
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA: Ages 18-75. Male or female. GERD symptoms at least twice a week for the last three months. Able to read, understand and complete study questionnaires and diary Understand the study procedures and sign written informed consent. Able to comply with all study requirements. EXCLUSION CRITERIA: Subjects with erosive esophagitis (EE), Barrett's esophagus (BE) and esophageal stricture or adenocarcinoma on upper endoscopy. Subjects with previous upper gastrointestinal surgery. Subjects with clinically significant medical conditions (cardiovascular, respiratory, renal, hepatic, hematologic, endocrine, neurologic and psychiatric); examples as follows: liver cirrhosis, severe COPD, severe renal failure, severe heart failure, active malignancy. Subjects requiring narcotics (morphine, methadone, etc.). Subjects requiring melatonin Subjects with diabetes, scleroderma and neuromuscular disorders. Lactating or pregnant women. Subjects with an unrecognized lifestyle such as shift workers.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ram M Dickman, MD
Phone
03:9377236
Email
dickmanr@clalit.org.il
First Name & Middle Initial & Last Name or Official Title & Degree
Tami Lederfine
Phone
03:9377040
Email
Tamila@clalit.org.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ram M Dickman, MD
Organizational Affiliation
Rabin Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rabin Medical Center, Beilinson Hospital
City
Petach Tikva
ZIP/Postal Code
49100
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ram M Dickman, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
16948779
Citation
Pereira Rde S. Regression of gastroesophageal reflux disease symptoms using dietary supplementation with melatonin, vitamins and aminoacids: comparison with omeprazole. J Pineal Res. 2006 Oct;41(3):195-200. doi: 10.1111/j.1600-079X.2006.00359.x.
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SThe Effects of Melatonin on GERD Symptoms

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