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NCT01288612 · ClinicalTrials.gov registry record · NA
Comparative Effectiveness of Endoscopic Assessment of Gastroesophageal Reflux and Barretts Esophagus
A NA study, sponsored by Mayo Clinic.
- Completed
- Registry status
- NA
- Development phase
- 459
- Enrollment target
NCT01288612: Completed NA study, sponsored by Mayo Clinic.
NCT01288612 is a NA study that has completed, run by Mayo Clinic. The registered enrollment target is 459 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01288612, a NA study, has completed, sponsored by Mayo Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 459 participants
- Enrollment target
Study Summary
The hypothesis of this study was that the comparative effectiveness of unsedated transnasal endoscopy (uTNE) will be greater than sedated endoscopy (sEGD) in population screening for BE.
Primary Outcome
This outcome measure was defined as the proportion of subjects who agreed to undergo esophageal assessment in the three groups out of those who were eligible to be contacted for participation in screening.
Interventions
- DEVICE Transnasal Endoscopy
- DEVICE Sedated Endoscopy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 459 participants |
| Start Date | 2011-02 |
| Est. Completion | 2013-10 |
| Phase | NA |
What the finished NCT01288612 record still lists
NCT01288612 is an interventional study that assigns participants to a tested intervention. The registered 459 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (67% lower).
The record links to 0 conditions, and to 2 interventions - of which Transnasal Endoscopy is the first listed.
NCT01288612 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01288612 about?
NCT01288612 is a clinical study titled "Comparative Effectiveness of Endoscopic Assessment of Gastroesophageal Reflux and Barretts Esophagus". The hypothesis of this study was that the comparative effectiveness of unsedated transnasal endoscopy (uTNE) will be greater than sedated endoscopy (sEGD) in population screening for BE.
What is the current status of trial NCT01288612?
This trial is currently completed. It is a NA study. The enrollment target is 459 participants. The study started on 2011-02. Estimated completion is 2013-10.
What interventions are being tested in trial NCT01288612?
The interventions under investigation include: Transnasal Endoscopy (DEVICE), Sedated Endoscopy (DEVICE).
Who is sponsoring clinical trial NCT01288612?
This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01288612's enrollment target sits among peer trials
459 224th of 2000 higher than 1,777 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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