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NCT07633847 · ClinicalTrials.gov registry record

A Post Market Trial Assessing the Accuracy of Normal Mode Reading vs. ProScan Reading With the NaviCam SB System. This is a Comparison of Retrospectively Obtained Capsule Endoscopy Videos With a New AI Reading Tool; no New Interventions Will be Completed.

A clinical trial, sponsored by AnX Robotica.

Not yet
Registry status
92
Enrollment target

NCT07633847: Clinical Trial study, sponsored by AnX Robotica.

NCT07633847 is a clinical trial that has not yet begun recruiting, run by AnX Robotica. The registered enrollment target is 92 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07633847 has not yet begun recruiting, sponsored by AnX Robotica.

NOT YET RECRUITING
Registry status
92 participants
Enrollment target

Study Summary

NaviCam ProScan is an artificial intelligent (AI) assisted reading tool designed to aid small bowel capsule endoscopy reviewers in decreasing the time to review capsule endoscopy images for adult patients in whom the capsule endoscopy images were obtained for suspected small bowel bleeding.

Primary Outcome

Subject-level sensitivity will be evaluated for superiority of ProScan assistance versus unassisted assessments in the identification of patients with one or more true findings.

Interventions

  • DEVICE Video capsule endoscopy
  • OTHER Phase II = Data analysis by Independent Readers
  • OTHER Phase III = Data Analysis by Expert Readers

Trial Details

FieldValue
Enrollment Target 92 participants
Start Date 2026-06-15
Est. Completion 2028-09-15
AnX Robotica

3 total trials

What is known before NCT07633847 opens enrollment

NCT07633847 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 92 participants, a relatively small participant target.

The record links to 0 conditions, and to 3 interventions - of which Video capsule endoscopy is the first listed.

NCT07633847 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07633847 about?

NCT07633847 is a clinical study titled "A Post Market Trial Assessing the Accuracy of Normal Mode Reading vs. ProScan Reading With the NaviCam SB System. This is a Comparison of Retrospectively Obtained Capsule Endoscopy Videos With a New AI Reading Tool; no New Interventions Will be Completed.". NaviCam ProScan is an artificial intelligent (AI) assisted reading tool designed to aid small bowel capsule endoscopy reviewers in decreasing the time to review capsule endoscopy images for adult patients in whom the capsule endoscopy images were obtained for suspected small bowel bleeding.

What is the current status of trial NCT07633847?

This trial is currently not yet recruiting. The enrollment target is 92 participants. The study started on 2026-06-15. Estimated completion is 2028-09-15.

What interventions are being tested in trial NCT07633847?

The interventions under investigation include: Video capsule endoscopy (DEVICE), Phase II = Data analysis by Independent Readers (OTHER), Phase III = Data Analysis by Expert Readers (OTHER).

Who is sponsoring clinical trial NCT07633847?

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

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Source: ClinicalTrials.gov NCT07633847, the US trial registry maintained by the National Library of Medicine. NCT07633847 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.