Effect of Pantoprazole 40mg Daily vs Placebo on Power Spectral Analysis of the Sleep EEG of Patients With GERD.

Sponsor
Southern Arizona VA Health Care System (U.S. Fed)
Overall Status
Completed
CT.gov ID
NCT00674245
Collaborator
(none)
40
1
2
27
1.5

Study Details

Study Description

Brief Summary

The purpose of this research study is to determine if treatment with pantoprazole 40 mg daily versus a placebo improves sleep quality in patients with gastroesophageal reflux disease (GERD). Another purpose is to determine if treatment with pantoprazole 40 mg once daily versus a placebo improves sleep outcomes in patients with gastroesophageal reflux disease using spectral analysis of sleep electroencephalogram (EEG).

Condition or Disease Intervention/Treatment Phase
Phase 2/Phase 3

Detailed Description

It appears that the presence of intraesophageal stimuli alone may not be sufficient to elicit symptoms of heartburn. Most acid reflux events (>80%-90%) do not reach conscious level and thus are not perceived.[3] It is yet to be determined what factors enhance our perception of esophageal stimuli and may help to elevate them to the conscious level. In recent years, central and peripheral factors that may enhance our perception of intraesophageal stimuli have been evaluated. Intraduodenal fat infusion was shown to enhance perception of intraesophageal acid in patients with GERD.[4] This study suggested that fat is an important modulator of postprandial GERD symptoms. Central factors, such as stress and psychological comorbidity, also appear to have an important role in symptom generation in patients with GERD, regardless if esophageal inflammation is present or absent.[5-8] Thus, by modulating brain-gut interactions, perception of pathological and probably physiological events in the esophagus of patients with GERD may be altered.

Poor sleep is a central factor that may enhance perception of intraesophageal stimuli and thus elevate them to the conscious level. Several studies have demonstrated that patients with fibromyalgia or irritable bowel syndrome report increased symptoms due to sleep abnormalities.[9, 10] Similar reports in patients with GERD are not available. A subset of patients with GERD experience nocturnal heartburn that may awaken them during the night. In others, despite lack of nocturnal symptoms, sleep abnormalities may occur due to acid reflux events. In both cases, GERD leads to poor sleep, and that in turn may enhance perception of intraesophageal stimuli, leading to reports of increased frequency and severity of perceived GERD symptoms. Thus, poor sleep may be a crucial factor in symptom generation and exacerbation of patients with GERD.

Recently, we have used a novel technique, power spectral analysis of the sleep electroencephalogram (EEG), to assess patients with heartburn and erosive esophagitis and those with heartburn but without erosive esophagitis.[11] We were able to show that among heartburn patients with GERD, EEG spectral power during sleep is shifted towards higher frequencies as compared to heartburn patients without GERD despite similar sleep architecture.

Several recent therapeutic trials in GERD patients have failed to demonstrate improvement in polysomnographic studies despite improvement in GERD-related symptoms and subjective reports of sleep quality.[12] Spectral analysis of the sleep EEG might be a more sensitive tool than polysomnographic study in assessing objective improvement of sleep in patients receiving antireflux treatment.

In summary, sleep disturbances in patients with GERD are poorly recognized and rarely elicited during clinic visits despite their significant impact on patients' quality of life and probably perception of disease severity. Several studies have demonstrated improvement of subjective reports of sleep quality in patients with GERD receiving antireflux treatment. However, the effect of potent antireflux therapy on objective sleep parameters has yet to be demonstrated.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effect Of Pantoprazole 40 mg Once Daily Versus Placebo On The Power Spectral Analysis Of The Sleep Electroencephalogram (EEG) Of Patients With Gastroesophageal Reflux Disease (GERD)
Study Start Date :
Apr 1, 2008
Actual Primary Completion Date :
Jul 1, 2010
Actual Study Completion Date :
Jul 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Pantoprazole

40 mg once daily for four weeks improves sleep quality in patients with GERD

Drug: Pantoprazole
40 mg once daily for 4 weeks
Other Names:
  • Protonix
  • PPI
  • Drug: Pantoprazole
    40 mg once daily improves sleep quality in patients with GERD.
    Other Names:
  • Protonix
  • PPI
  • Placebo Comparator: placebo

    To determine if treatment with pantoprazole 40 mg once daily vs placebo improves sleep outcome in patients with GERD.

    Drug: placebo
    40 mg once daily for 4 weeks
    Other Names:
  • sugar pill
  • Outcome Measures

    Primary Outcome Measures

    1. Symptom control after 4 weeks of treatment. [April 2008 to July 2010]

      To determine if treatment with pantoprazole 40 mg daily vs placebo improves sleep quality in patients with GERD.

    Secondary Outcome Measures

    1. Effect of Pantoprazole 40 mg Daily vs Placebo on the Power Spectral Analysis of the Sleep Electroencephalogram of Patients With GERD. [April 2008-July 2010]

      To determine if treatment with pantoprazole 40 mg once daily vs placebo improves sleep outcome in patients with GERD using spectral analysis of sleep electroencephalogram.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 18 to 80 yrs of age

    • 2 to 3 episodes of GERD/week

    • erosive esophagitis or abnormal 24 hr pH

    • able to read and understand, complete questionnaires

    Exclusion Criteria:
    • barrett's esophagus or peptic stricture on endoscopy

    • normal EGD and normal 24 hour pH

    • previous upper GI surgery

    • comorbidity (cardiovascular, respiratory, renal, hepatic)

    • use of narcotics or pain medication on regular basis

    • insomnia, shift work sleep disorder, sleep apnea, restless leg syndrome

    • diabetes, scleroderma or neuromuscular disorders

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Southern Arizona VA Health Care System Tucson Arizona United States 85723

    Sponsors and Collaborators

    • Southern Arizona VA Health Care System

    Investigators

    • Principal Investigator: Ronnie Fass, MD, Southern VA Health Care System

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00674245
    Other Study ID Numbers:
    • 08-0001-01 & R&D#00-77
    First Posted:
    May 7, 2008
    Last Update Posted:
    Aug 19, 2010
    Last Verified:
    Aug 1, 2010

    Study Results

    No Results Posted as of Aug 19, 2010