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NCT03349112 · ClinicalTrials.gov registry record · NA
Study: Manometry With & Without Lidocaine
A NA study of Normal, sponsored by University of Wisconsin, Madison.
- Completed
- Registry status
- NA
- Development phase
- 36
- Enrollment target
- 1
- Study location
NCT03349112: Completed NA study of Normal, sponsored by University of Wisconsin, Madison.
NCT03349112 is a NA study of Normal that has completed, run by University of Wisconsin, Madison. The registered enrollment target is 36 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03349112, a NA study of Normal, has completed, sponsored by University of Wisconsin, Madison.
- COMPLETED
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine whether subjects report a difference in comfort with High Resolution Pharyngeal Manometry (HRPM) conducted following application of lidocaine as an anesthetic as compared to HRPM conducted without anesthetic.
Primary Outcome
Following HRPM without additional lidocaine and following HRPM with additional lidocaine, the subject will be asked to rate their level of comfort during the procedure using a visual analog scale.
Conditions Studied
Interventions
- BEHAVIORAL 4% Lidocaine Spray
- BEHAVIORAL 2% Viscous Lidocaine
Study Locations (1)
Wisconsin
- University of Wisconsin - Madison - Madison
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2015-12-22 |
| Est. Completion | 2018-11-09 |
| Phase | NA |
What the finished NCT03349112 record still lists
NCT03349112 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 1 condition, with Normal appearing as the primary indexed condition, and to 2 interventions - of which 4% Lidocaine Spray is the first listed.
NCT03349112 reports a single indexed study location in Wisconsin.
Frequently Asked Questions
What is clinical trial NCT03349112 about?
NCT03349112 is a clinical study titled "Study: Manometry With & Without Lidocaine". The purpose of this study is to determine whether subjects report a difference in comfort with High Resolution Pharyngeal Manometry (HRPM) conducted following application of lidocaine as an anesthetic as compared to HRPM conducted without anesthetic.
What is the current status of trial NCT03349112?
This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2015-12-22. Estimated completion is 2018-11-09.
What conditions does trial NCT03349112 study?
This clinical trial studies the following conditions: Normal.
What interventions are being tested in trial NCT03349112?
The interventions under investigation include: 4% Lidocaine Spray (BEHAVIORAL), 2% Viscous Lidocaine (BEHAVIORAL).
Who is sponsoring clinical trial NCT03349112?
This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03349112 being conducted?
This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03349112's enrollment target sits among peer trials
36 1541st of 2000 higher than 437 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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