Pantoprazole 20/40 mg in the Treatment of Symptomatic Reflux Disease With Focus on Sleep Disorders

Overview[ - collapse ][ - ]

Purpose The aim of the study was to evaluate the effect of pantoprazole on sleep disorders in patients with NERD (non-erosive reflux disease) or eGERD (erosive gastroesophageal reflux disease). The prevalence and intensity of the sleep disorders were evaluated by a standardized questionnaire. The study was expected to provide further data on safety and tolerability of pantoprazole.
ConditionSleep Disorders
Non-Erosive Reflux Disease
Gastroesophageal Reflux Disease
InterventionDrug: Pantoprazole
PhaseN/A
SponsorNycomed
Responsible PartyNycomed
ClinicalTrials.gov IdentifierNCT00830115
First ReceivedJanuary 13, 2009
Last UpdatedMay 4, 2012
Last verifiedMay 2012

Tracking Information[ + expand ][ + ]

First Received DateJanuary 13, 2009
Last Updated DateMay 4, 2012
Start DateJanuary 2009
Estimated Primary Completion DateJune 2009
Current Primary Outcome Measures
  • Patient's Assessment of Stanford Sleepiness Scale for the Last 24 Hours (Diaries) [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale from 1=Feeling active, vital, alert, or wide awake to 7=No longer fighting sleep, sleep onset soon, having dream-like thoughts
  • Patient's Assessment of Sleep Disturbances for the Last 24 Hours (Diaries) [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: Severity from 1=Not impaired to 10=Severely impaired
  • Physician's Assessment of Sleep Disturbances [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: 1=none, 2=mild, 3=moderate, 4=severe
Current Secondary Outcome Measures
  • Patient's Assessment of General Well-being for the Last 24 Hours (Diaries) [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: Severity from 1=Excellent to 10=Extremely bad
  • Patient's Assessment of Acid Complaints for the Last 24 Hours (Diaries) [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: Severity from 1=Not impaired to 10=Severely impaired
  • Patient's Assessment of Upper-abdominal/Stomach Complaints for the Last 24 Hours (Diaries) [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: Severity from 1=Not impaired to 10=Severely impaired
  • Patient's Assessment of Lower Abdominal/Digestive Complaints for the Last 24 Hours (Diaries) [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: Severity from 1=Not impaired to 10=Severely impaired
  • Patient's Assessment of Nausea for the Last 24 Hours (Diaries) [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: Severity from 1=Not impaired to 10=Severely impaired
  • Physician's Assessment of Heartburn [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: 1=none, 2=mild, 3=moderate, 4=severe
  • Physician's Assessment of Acid Eructation [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: 1=none, 2=mild, 3=moderate, 4=severe
  • Physician's Assessment of Painful Swallowing [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: 1=none, 2=mild, 3=moderate, 4=severe
  • Assessment of the Efficacy of Pantoprazole at Final Visit [Time Frame: 7 days] [Designated as safety issue: No]Assessment on a scale: 1=excellent, 2=good, 3=satisfactory, 4=not satisfactory
  • Assessment of the Tolerability of Pantoprazole at Final Visit [Time Frame: 7 days] [Designated as safety issue: Yes]Assessment on a scale: 1=excellent, 2=good, 3=satisfactory, 4=not satisfactory

Descriptive Information[ + expand ][ + ]

Brief TitlePantoprazole 20/40 mg in the Treatment of Symptomatic Reflux Disease With Focus on Sleep Disorders
Official TitleEfficacy of Pantoprazole in Patients Older Than 12 Years With Reflux Associated Sleep Disorders
Brief Summary
The aim of the study was to evaluate the effect of pantoprazole on sleep disorders in
patients with NERD (non-erosive reflux disease) or eGERD (erosive gastroesophageal reflux
disease). The prevalence and intensity of the sleep disorders were evaluated by a
standardized questionnaire. The study was expected to provide further data on safety and
tolerability of pantoprazole.
Detailed DescriptionNot Provided
Study TypeObservational
Study PhaseN/A
Study DesignObservational Model: Case-Only, Time Perspective: Prospective
Condition
  • Sleep Disorders
  • Non-Erosive Reflux Disease
  • Gastroesophageal Reflux Disease
InterventionDrug: Pantoprazole
Observational, non-interventional study (NIS). The physician decided about dosage according to individual needs (20 or 40 mg pantoprazole, once daily).
Study Arm (s)Pantoprazole
All patients enrolled

Recruitment Information[ + expand ][ + ]

Recruitment StatusCompleted
Estimated Enrollment1045
Estimated Completion DateJune 2009
Estimated Primary Completion DateMay 2009
Eligibility Criteria
Main inclusion criteria:

- Outpatients with erosive gastro-esophageal reflux disease (eGERD) or non-erosive
reflux disease (NERD)

Main exclusion criteria:

- Criteria as defined in the respective Summary of Product Characteristics (Chapter
4.3)
GenderBoth
Ages12 Years
Accepts Healthy VolunteersNo
ContactsNot Provided
Location CountriesGermany

Administrative Information[ + expand ][ + ]

NCT Number NCT00830115
Other Study ID NumbersP2-9999-010-DE
Has Data Monitoring CommitteeNo
Information Provided ByNycomed
Study SponsorNycomed
CollaboratorsNot Provided
Investigators Study Director: Thomas Bethke, MD, MBA Nycomed Deutschland GmbH, 78467 Konstanz, Germany
Verification DateMay 2012

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Nycomed Deutschland GmbH
Aachen, Germany, 52078
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Ahrensburg, Germany, 22926
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Altenburg, Germany, 04600
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