An Open-Label Trial of Dexlansoprazole 60mg for the Relief of Heartburn During the Fasting Month of Ramadan
Primary Purpose
GERD, Proton Pump Inhibitor
Status
Completed
Phase
Phase 4
Locations
Lebanon
Study Type
Interventional
Intervention
Dexlansoprazole 60 MG
Sponsored by
About this trial
This is an interventional treatment trial for GERD
Eligibility Criteria
Inclusion Criteria:
- Individuals 18-75 years old
- Fasting in Ramadan
- No daily PPI use
- Individuals willing to sign consent form
- Patients owning a smartphone and able to use a smartphone application
Exclusion Criteria:
- Known erosive GERD on PPI
- Pregnant females
- Prior gastric surgery
- Long standing diabetes mellitus (≥10 years of disease)
- Frequent NSAID use (>3x/week)
- Morbid obesity (BMI>35)
- History of recent (<6 months) upper GI bleeding
- Patients who do not own a smartphone or who cannot use a smartphone application
- Known allergy to PPIs
- Known history of poor compliance or adherence and active psychological problems which might impact adherence
Sites / Locations
- American University of Beirut - Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
1
Arm Description
34 patients will be assigned to take Dexlansoprazole 60mg over the 2nd, 3rd, and 4th weeks of the month of Ramadan.
Outcomes
Primary Outcome Measures
Heartburn Relief
The mean number of days during Ramadan with complete relief of heartburn symptoms, including nocturnal symptoms.
Secondary Outcome Measures
Days with partial relief of heartburn symptoms
Days with partial relief of heartburn symptoms
Days with relief of nocturnal heartburn symptoms
Days with relief of nocturnal heartburn symptoms
Improvement in sleep qualit
The number of nocturnal sleeping hours will be assessed daily
Side effects/tolerability of Dexlansoprazole 30mg vs. Dexlansoprazole 60mg
"Side effects and tolerability" Questionnaire
Full Information
NCT ID
NCT03079050
First Posted
February 27, 2017
Last Updated
September 14, 2017
Sponsor
American University of Beirut Medical Center
Collaborators
Takeda
1. Study Identification
Unique Protocol Identification Number
NCT03079050
Brief Title
An Open-Label Trial of Dexlansoprazole 60mg for the Relief of Heartburn During the Fasting Month of Ramadan
Official Title
An Open-Label Trial of Dexlansoprazole 60mg for the Relief of Heartburn During the Fasting Month of Ramadan
Study Type
Interventional
2. Study Status
Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
February 27, 2017 (Actual)
Primary Completion Date
July 30, 2017 (Actual)
Study Completion Date
July 30, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
American University of Beirut Medical Center
Collaborators
Takeda
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Dexlansoprazole modified release (MR), the R-enantiomer of Lansoprazole, is an FDA approved drug (2009) for the management of erosive esophagitis and nonerosive reflux disease 1. Dexlansoprazole has a unique dual delayed-release delivery system designed to address unmet needs that may accompany traditional proton pump inhibitors, with two separate pH-depended release phases, the first in the proximal duodenum and the second in the more distal small intestine. This dual release system extends the plasma concentration and pharmacodynamics effects beyond those of single-release PPIs, allowing for dosing at any time of the day without regard to meals 1. A study conducted by Fass et al. has shown that the use of dexlansoprazole MR 30 mg in patients with symptomatic GERD is significantly more effective than placebo in improving nocturnal heartburn, reducing GERD-related sleep disturbances, and consequently improving work productivity, sleep quality and quality of life 2.
Because of its pharmacokinetic properties, Dexlansoprazole modified release (MR) may prove beneficial in optimizing the management of GERD and the associated burdens that often surface after the heavy evening and Suhur meals, such as increased nocturnal symptoms and poor sleep quality.
Detailed Description
To investigate the efficacy and quality of life improvement of Dexlansoprazole 60mg taken once daily at Iftar time in patients with known symptomatic heartburn exacerbated in Ramadan and who are not on daily treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
GERD, Proton Pump Inhibitor
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
33 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
34 patients will be assigned to take Dexlansoprazole 60mg over the 2nd, 3rd, and 4th weeks of the month of Ramadan.
Intervention Type
Drug
Intervention Name(s)
Dexlansoprazole 60 MG
Other Intervention Name(s)
Dexilant 60 MG
Intervention Description
This drug will be given to 34 random patients during the 2nd, 3rd, and 4th weeks of the month of Ramadan to assess its ability to relieve GERD symptoms
Primary Outcome Measure Information:
Title
Heartburn Relief
Description
The mean number of days during Ramadan with complete relief of heartburn symptoms, including nocturnal symptoms.
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Days with partial relief of heartburn symptoms
Description
Days with partial relief of heartburn symptoms
Time Frame
1 month
Title
Days with relief of nocturnal heartburn symptoms
Description
Days with relief of nocturnal heartburn symptoms
Time Frame
1 month
Title
Improvement in sleep qualit
Description
The number of nocturnal sleeping hours will be assessed daily
Time Frame
1 month
Title
Side effects/tolerability of Dexlansoprazole 30mg vs. Dexlansoprazole 60mg
Description
"Side effects and tolerability" Questionnaire
Time Frame
1 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Individuals 18-75 years old
Fasting in Ramadan
No daily PPI use
Individuals willing to sign consent form
Patients owning a smartphone and able to use a smartphone application
Exclusion Criteria:
Known erosive GERD on PPI
Pregnant females
Prior gastric surgery
Long standing diabetes mellitus (≥10 years of disease)
Frequent NSAID use (>3x/week)
Morbid obesity (BMI>35)
History of recent (<6 months) upper GI bleeding
Patients who do not own a smartphone or who cannot use a smartphone application
Known allergy to PPIs
Known history of poor compliance or adherence and active psychological problems which might impact adherence
Facility Information:
Facility Name
American University of Beirut - Medical Center
City
Beirut
Country
Lebanon
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
21780890
Citation
Behm BW, Peura DA. Dexlansoprazole MR for the management of gastroesophageal reflux disease. Expert Rev Gastroenterol Hepatol. 2011 Aug;5(4):439-45. doi: 10.1586/egh.11.37.
Results Reference
background
PubMed Identifier
21224838
Citation
Fass R, Johnson DA, Orr WC, Han C, Mody R, Stern KN, Pilmer BL, Perez MC. The effect of dexlansoprazole MR on nocturnal heartburn and GERD-related sleep disturbances in patients with symptomatic GERD. Am J Gastroenterol. 2011 Mar;106(3):421-31. doi: 10.1038/ajg.2010.458. Epub 2011 Jan 11.
Results Reference
background
PubMed Identifier
22155561
Citation
Fass R, Inadomi J, Han C, Mody R, O'Neil J, Perez MC. Maintenance of heartburn relief after step-down from twice-daily proton pump inhibitor to once-daily dexlansoprazole modified release. Clin Gastroenterol Hepatol. 2012 Mar;10(3):247-53. doi: 10.1016/j.cgh.2011.11.021. Epub 2011 Dec 7.
Results Reference
background
PubMed Identifier
24632930
Citation
Solem C, Mody R, Stephens J, Macahilig C, Gao X. Mealtime-related dosing directions for proton-pump inhibitors in gastroesophageal reflux disease: physician knowledge, patient adherence. J Am Pharm Assoc (2003). 2014 Mar-Apr;54(2):144-53. doi: 10.1331/JAPhA.2014.13117.
Results Reference
background
PubMed Identifier
18789939
Citation
Kahrilas PJ, Shaheen NJ, Vaezi MF, Hiltz SW, Black E, Modlin IM, Johnson SP, Allen J, Brill JV; American Gastroenterological Association. American Gastroenterological Association Medical Position Statement on the management of gastroesophageal reflux disease. Gastroenterology. 2008 Oct;135(4):1383-1391, 1391.e1-5. doi: 10.1053/j.gastro.2008.08.045. No abstract available.
Results Reference
background
PubMed Identifier
26013794
Citation
Abbas Z. Gastrointestinal health in Ramadan with special reference to diabetes. J Pak Med Assoc. 2015 May;65(5 Suppl 1):S68-71.
Results Reference
background
PubMed Identifier
30625462
Citation
Rimmani HH, Rustom LBO, Rahal MA, Shayto RH, Chaar H, Sharara AI. Dexlansoprazole is Effective in Relieving Heartburn during the Fasting Month of Ramadan. Dig Dis. 2019;37(3):188-193. doi: 10.1159/000496091. Epub 2019 Jan 9.
Results Reference
derived
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An Open-Label Trial of Dexlansoprazole 60mg for the Relief of Heartburn During the Fasting Month of Ramadan
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