Capillary Endoscopy Aspiration Catheter for Microbiota and SIBO

This study is testing a new device called the Capillary Endoscopy Aspiration Catheter. It's designed to collect fluid from your small intestine more efficiently during an upper endoscopy (a procedure where a thin, flexible tube with a camera is used to look inside your digestive tract). The goal is to see if this new catheter can collect more fluid and do it faster than the standard Endoscopy Aspiration Catheter. Researchers are interested in improving how we study the small intestine's microbiota (the community of microorganisms living there) and conditions like SIBO (Small Intestinal Bacterial Overgrowth). You could join if you are between 18 and 85 years old and are already scheduled for an upper endoscopy. The study will measure the amount of fluid collected and how long it takes, over 5 minutes.

Study design
This study is comparing two different catheters in 46 participants. Each participant will receive either the standard catheter or the new capillary catheter during their endoscopy.
What's involved
You would undergo an endoscopy procedure as part of your regular medical care. During this procedure, either the standard or investigational catheter will be used to collect a small amount of fluid.
Compensation
Not stated in the trial record.
Follow-up
The primary measurements for this study are taken at 5 minutes during the aspiration process.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT04418258

Capillary Endoscopy Aspiration Catheter

Recruiting
NAAges 18–85InterventionalHealth services
Cedars-Sinai Medical Center
~46 participants
Updated 2026-01-26 on ClinicalTrials.gov
What's tested:Capillary Endoscopy Aspiration CatheterEndoscopy Aspiration Catheter

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
The volume(millilitres) of the aspirate that will be suctioned from small intestine in two groups
Measured over 5 minutes
+1 more outcome measured
Microbiota
SIBO

NCT04418258

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Cedars-Sinai Medical Center

    Los Angeles, Californiastudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Ali Rezaie, MD · PRINCIPAL_INVESTIGATOR · Cedars-Sinai Medical Center

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Eligibility criteria

Inclusion

Male or female subjects aged 18-85 undergoing esophagogastroduodenoscopy.
  • The volume(millilitres) of the aspirate that will be suctioned from small intestine in two groups5 minutes

    The volume(millilitres) of the aspirate that collected from small intestine during upper endoscopy will be the primary end point

  • The time(minutes) of the aspirate collection from small intestine will be measured in two groups5 minutes

    The time(minutes) of the aspirate collection from small intestine will be measured in two groups