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NCT04605302 · ClinicalTrials.gov registry record · NA

Comparative Study of MCCE With/Without Tether vs Conventional Upper Endoscopy in Patients With Upper Abdominal Symptoms

A NA study of Upper Gastrointestinal Symptoms, sponsored by AnX Robotica.

Completed
Registry status
NA
Development phase
27
Enrollment target
1
Study location

NCT04605302 is a NA study of Upper Gastrointestinal Symptoms that has completed, run by AnX Robotica. The registered enrollment target is 27 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT04605302, a NA study of Upper Gastrointestinal Symptoms, has completed, sponsored by AnX Robotica.

COMPLETED
Registry status
NA
Development phase
27 participants
Enrollment target
1
Study location

Study Summary

A prospective single blinded, tandem study, comparing a magnetically controlled capsule with or without a tether (MCC or MCC-T) with conventional upper endoscopy for the diagnosis of patients with upper abdominal symptoms.

Interventions

  • DEVICE MCC/MCC-T
  • DEVICE Standard gastroscopy

Study Locations (1)

Massachusetts

  • University of Massachusetts Medical School - Worcester

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2021-02-10
Est. Completion 2023-03-30
Phase NA

Sponsor

AnX Robotica

3 total trials

What the Registry Record Tells You About NCT04605302

The ClinicalTrials.gov registry entry for NCT04605302 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 27 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AnX Robotica, which has 3 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Upper Gastrointestinal Symptoms appearing as the primary indexed condition, and to 2 interventions - of which MCC/MCC-T is the first listed.

NCT04605302 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT04605302 about?

NCT04605302 is a clinical study titled "Comparative Study of MCCE With/Without Tether vs Conventional Upper Endoscopy in Patients With Upper Abdominal Symptoms". A prospective single blinded, tandem study, comparing a magnetically controlled capsule with or without a tether (MCC or MCC-T) with conventional upper endoscopy for the diagnosis of patients with upper abdominal symptoms.

What is the current status of trial NCT04605302?

This trial is currently completed. It is a NA study. The enrollment target is 27 participants. The study started on 2021-02-10. Estimated completion is 2023-03-30.

What conditions does trial NCT04605302 study?

This clinical trial studies the following conditions: Upper Gastrointestinal Symptoms.

What interventions are being tested in trial NCT04605302?

The interventions under investigation include: MCC/MCC-T (DEVICE), Standard gastroscopy (DEVICE).

Who is sponsoring clinical trial NCT04605302?

This trial is sponsored by AnX Robotica, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04605302 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.