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OpenTrials
Completed

NCT Number: NCT00867204

Short Versus Long Wire ERCP Systems

This study looked at short-wire ERCP devices versus Long-wire ERCP devices. The study hypothesis is to compare the performance of the Fusion ERCP short-wire system to the traditional Long-wire system.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Florida/Shands UF Endoscopy Center

Gainesville, Florida, 32610, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients undergoing ERCP.

Exclusion criteria

  • Age less than 18 years, pregnant women, patients unable to provide informed concent, prior surgery causing a significant change in the anatomy of the papilla (Billroth II or Roux-en-Y)

Treatment and study plan

ERCP

Procedure

Patients with clinical indication for ERCP were invited to participate in the Study

Primary outcomes

  1. Time for device exchange and stent insertion

    Time frame: during the ERCP

Sponsors and collaborators

Lead sponsor

University of Florida

Other

Registry information

Official study title

Prospective Randomized Blinded Comparison of a Short-wire ERCP System to Traditional Long-wire Devices

Acronym: ERCP systems

Important dates

Study start
2004
Primary completion
2008
Study completion
2009
First posted
Mar 23, 2009
Registry last updated
Sep 20, 2011

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.

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