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NCT02729753 · ClinicalTrials.gov registry record · NA

Clinical Study to Evaluate CryoBalloon™ Full and Swipe Ablation Systems for Ablation of Human Esophageal Epithelium

A NA study of Esophageal Cancer, sponsored by Pentax Medical.

Completed
Registry status
NA
Development phase
10
Enrollment target
2
Study locations

NCT02729753 is a NA study of Esophageal Cancer that has completed, run by Pentax Medical. The registered enrollment target is 10 participants, below the 499-participant average among 123 other Esophageal Cancer trials with a reported enrollment target (98% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT02729753, a NA study of Esophageal Cancer, has completed, sponsored by Pentax Medical.

COMPLETED
Registry status
NA
Development phase
10 participants
Enrollment target
2
Study locations

Study Summary

This study will evaluate the C2 CryoBalloon™ Full and Swipe Ablation Systems for the ablation of human esophageal epithelium in patients scheduled to undergo esophagectomy for reasons unrelated to the objective of the study

Conditions Studied

Interventions

  • DEVICE CryoBalloon™ Full Ablation System
  • DEVICE CryoBalloon™ Swipe Ablation System

Study Locations (2)

Texas

  • MD Anderson Cancer Center - Houston

Washington

  • Swedish Medical Center and Cancer Institute - Seattle

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2016-04
Est. Completion 2016-10-30
Phase NA

Sponsor

Pentax Medical

4 total trials

What the Registry Record Tells You About NCT02729753

The ClinicalTrials.gov registry entry for NCT02729753 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 499-participant average among 123 other Esophageal Cancer trials with a reported enrollment target (98% lower). The listed sponsor is Pentax Medical, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Esophageal Cancer appearing as the primary indexed condition, and to 2 interventions - of which CryoBalloon™ Full Ablation System is the first listed.

NCT02729753 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Texas, Washington.

Frequently Asked Questions

What is clinical trial NCT02729753 about?

NCT02729753 is a clinical study titled "Clinical Study to Evaluate CryoBalloon™ Full and Swipe Ablation Systems for Ablation of Human Esophageal Epithelium". This study will evaluate the C2 CryoBalloon™ Full and Swipe Ablation Systems for the ablation of human esophageal epithelium in patients scheduled to undergo esophagectomy for reasons unrelated to the objective of the study

What is the current status of trial NCT02729753?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2016-04. Estimated completion is 2016-10-30.

What conditions does trial NCT02729753 study?

This clinical trial studies the following conditions: Esophageal Cancer.

What interventions are being tested in trial NCT02729753?

The interventions under investigation include: CryoBalloon™ Full Ablation System (DEVICE), CryoBalloon™ Swipe Ablation System (DEVICE).

Who is sponsoring clinical trial NCT02729753?

This trial is sponsored by Pentax Medical, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02729753 being conducted?

This trial has 2 study locations across Texas, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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