Translational Research Center for Gastrointestinal Disorders - KU Leuven
Leuven, Vlaams-Brabant, 3000, Belgium
NCT Number: NCT05264363
In order to validate that the VIPUN, Gastric Monitoring System (GMS) is a gastric motility monitoring system, we intend to show that the VIPUN GMS can assess motility through pressure measurement similar to high-resolution manometry (HRM).
In addition, the study aims to contribute to the design and development of a position confirmation functionality integrated in the VIPUN Gastric Monitoring System by establishing volume-pressure relations in the stomach and esophagus.
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Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Leuven, Vlaams-Brabant, 3000, Belgium
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The Investigational Medical Device (IMD) is used simultaneously with the reference device (solid state high-resolution manometry) to record gastric intraluminal pressure for approximately 2.5 hours.
Other names: VIPUN GMS
Time frame: protocol time T=0-120 minutes
Time the smoothed and baseline-corrected VIPUN GMS pressure exceeds the contraction-threshold.
Time frame: protocol time T=0-120 minutes
Time the smoothed and baseline-corrected gastric manometry pressure exceeds the contraction-threshold
Time frame: protocol time T=0-120 minutes
Gastric contractions identified visually by a expert gastroenterologists on the VIPUN GMS recording.
Time frame: protocol time T=0-120 minutes
Gastric contractions identified visually by a expert gastroenterologists on the manometry recording.
Time frame: protocol time T=0-120 minutes
Motility Tile Runner contractions are gastric contractions identified by the VIPUN Motility Tiled Runner software application.
Time frame: protocol time T=0-150 minutes
The presence/absence of hallmarks of normal gastric motility are scored by expert gastroenterologists on the VIPUN GMS pressure recording and on the manometry recording independently.
Time frame: protocol time T=0-150 minutes
The duration of MMC phase III is delineated by expert gastroenterologists on the VIPUN GMS pressure recording and on the manometry recording independently.
Time frame: protocol time T=0-150 minutes
Defined as the difference between baseline GMS pressure before and during nutrient administration.
Time frame: protocol time T=0-150 minutes
Defined as the difference between the frequency of Motility Tiled Runner contractions before and during nutrient administration.
Time frame: Prior to protocol time T=0 minutes (=start motility recording).
The pressure at each volume increment (range 0-135 ml) is recorded during stepwise inflation of the VIPUN GMS Catheter in the esophagus and in the stomach.
Time frame: Throughout the study visit, specifically at baseline, during stepwise inflation (at each volume increment), and during the motility recording (at protocol time T=0, 60, 120 and 150 minutes).
The severity of epigastric and nasopharyngeal symptoms are surveyed by means of a questionnaire throughout the study visit.
Time frame: Throughout study visit (from the moment the investigational medical device is applied until it is removed).
All adverse events and device deficiencies are recorded.
VIPUN Medical
Industry
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.