Evaluation of the Safety and Effectiveness of Tailored Transoral Incisionless Fundoplication (TIF) Using EsophyX for the Treatment of GERD
This study has been withdrawn prior to enrollment.
(No funding source for device purchasing)
Sponsor:
University of Alberta
Collaborator:
Alberta Health Services
Information provided by (Responsible Party):
Daniel Birch, University of Alberta
ClinicalTrials.gov Identifier:
NCT01025739
First received: December 2, 2009
Last updated: September 18, 2011
Last verified: September 2011
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No Study Results Posted on ClinicalTrials.gov for this Study
Study was withdrawn before participants were enrolled.
| Study Status: | This study has been withdrawn prior to enrollment. |
|---|---|
| Study Completion Date: | February 2011 |
| Primary Completion Date: | February 2011 (Final data collection date for primary outcome measure) |