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Completed

NCT Number: NCT00682877

A Comparison of SmartPill Capsule With Scintigraphy for Determining Gastric Residence Time - Over 65 Years Old

The purpose of this study is to determine the correlation between gastric residence time of the SmartPill Capsule and the time required for partial emptying of a standard radiolabeled meal as measured by gastric emptying scintigraphy for subjects 65 years of age and older.

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Key information

Age range

65 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Division of Gastroenterology and Hepatology at KUMC, Kansas City, Kansas, United States

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About this study

Gastric emptying scintigraphy is considered the gold standard for evaluating gastric emptying and is widely available. Accurate characterization of gastric emptying may guide medical and surgical treatment choices. In addition, these techniques may allow for monitoring of therapeutic results for follow-up patient management.

The SmartPill GI Monitoring System offers an alternative non-invasive method for characterizing disorders of the stomach. The system consists of an ingestible capsule that houses sensors for pH, temperature, and pressure, a receiver for receiving and storing signals from the capsule, and software for displaying data on a personal computer. The capsule samples at regular intervals and transmits the sensed pH, pressure, and temperature data to a portable receiver worn by the subject. After test completion, the recorded data is downloaded to a personal computer for subsequent evaluation. This trial is for subjects 65 years of age and older.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Inclusion Criteria For Healthy Subjects:
  • Healthy males and females between ages 65-80 years of age with no gastrointestinal disease as screened by the GI Disease Screening Questionnaire
  • Average bowel movement frequency of at least one bowel movement within 48 hours
  • Subjects with high probability for compliance and completion of the study
  • Inclusion Criteria For Subjects with Gastroparesis:
  • Abnormal gastric emptying as defined by local standards and documented by nuclear medicine scintigraphy performed within the last two years.
  • Males and females between ages 18-65 years of age.
  • Average bowel movement frequency of at least one bowel movement within 72 hours
  • Subjects with high probability for compliance and completion of the study
  • Upper endoscopy or upper GI within last 3 years showing no evidence of gastric bezoar, stricture, or peptic ulcer.

Exclusion criteria

  • Exclusion Criteria For Healthy Subjects:
  • Prior GI surgery
  • Surgery within the past 3 months
  • Diverticulitis
  • Tobacco use within eight hours prior to capsule ingestion and during the 8 hour monitoring time.
  • Alcohol use within 24 hours prior to capsule ingestion and throughout the entire monitoring period (up to 72 hours).
  • Body mass index (BMI) > 35
  • Allergies to components of the test meal including eggs, bread, and jam.
  • Female of childbearing age who is not practicing birth control and/or is pregnant or lactating. (Confirm with urine pregnancy test)
  • Cardiovascular, endocrine, renal, or other chronic disease likely to affect motility.
  • Exclusion Criteria For Subjects with Gastroparesis:
  • History of gastric bezoar
  • Severe dysphagia to solid food and pills
  • Severe vomiting more than 1 time per day
  • Diverticulitis
  • Severe daily abdominal pain requiring medications for relief
  • Severe weight loss, greater than 10 lbs over the preceding 2 months.
  • Uncontrolled diabetes with a hemoglobin A1C greater than 10.
  • Excessively delayed gastric emptying time: more than 90% of a standard egg meal retained after 2 hours.
  • Previous gastro-esophageal surgery including vagotomy, fundoplication, gastric bypass, ulcer surgery.
  • Prior GI surgery except for uncomplicated appendectomy and laparoscopic cholecystectomy
  • Surgery within the past 3 months
  • Tobacco use within eight hours prior to capsule ingestion and during the 8 hour monitoring time.
  • Alcohol use within 24 hours prior to capsule ingestion and throughout the entire monitoring period (up to 72 hours).
  • BMI > 35
  • Allergies to components of the test meal including eggs, bread, and jam
  • Female of childbearing age who is not practicing birth control and/or is pregnant or lactating. (Confirm with urine pregnancy test)

Treatment and study plan

Primary outcomes

  1. To demonstrate the correlation between the gastric residence time as determined by SmartPill GI Monitoring System and the gastric emptying time of a radiolabeled meal in both healthy subjects and patients with documented gastroparesis.

    Time frame: 30 minute intervals up to 6 hours

Secondary outcomes

  1. To demonstrate that the gastric residence time as determined by SmartPill GI Monitoring System can discriminate between healthy human subjects and patients with gastroparesis

    Time frame: Continuous time measure until capsule elimination

  2. To characterize pressure patterns within the antrum and duodenum in healthy subjects and patients with documented gastroparesis

    Time frame: Continuous time measure until capsule elimination

  3. To characterize total GI transit time in healthy subjects

    Time frame: Continuous time measure until capsule elimination

Sponsors and collaborators

Lead sponsor

The SmartPill Corporation

Industry

Registry information

Official study title

A Comparison Trial of SmartPill Corporation GI Monitoring System With Scintigraphic Gastric Emptying Procedure for Determining Gastric Residence Time - In Subjects Over 65 Years of Age

Acronym: GETOver65

Important dates

Study start
2007
Primary completion
2007
Study completion
2007
First posted
May 23, 2008
Registry last updated
May 23, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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