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NCT01876706 · ClinicalTrials.gov registry record · NA

UroLift System TOlerability and ReCovery When Administering Local Anesthesia

A NA study, sponsored by NeoTract.

Completed
Registry status
NA
Development phase
51
Enrollment target

NCT01876706: Completed NA study, sponsored by NeoTract.

NCT01876706 is a NA study that has completed, run by NeoTract. The registered enrollment target is 51 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01876706, a NA study, has completed, sponsored by NeoTract.

COMPLETED
Registry status
NA
Development phase
51 participants
Enrollment target

Study Summary

The purpose of the study is to evaluate procedure tolerability and surgical recovery following the UroLift® system procedure when conducted with local anesthesia in subjects with symptomatic benign hyperplasia (BPH). Primary effectiveness will be achieved by looking at the Quality of Recovery Visual Analog Scale (QoR VAS) by the one month follow-up visit.

Primary Outcome

Primary effectiveness will be achieved when 80% (95% lower confidence limit) of subjects achieve a score of 80 or more on the Quality of Recovery Visual Analog Scale (QoR VAS) by the one month follow-up visit. The VAS scale is 0-100, with 100 being 100% recovery.

Interventions

  • DEVICE UroLift® System

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2013-04
Est. Completion 2018-09-04
Phase NA
NeoTract

4 total trials

What the finished NCT01876706 record still lists

NCT01876706 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which UroLift® System is the first listed.

NCT01876706 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01876706 about?

NCT01876706 is a clinical study titled "UroLift System TOlerability and ReCovery When Administering Local Anesthesia". The purpose of the study is to evaluate procedure tolerability and surgical recovery following the UroLift® system procedure when conducted with local anesthesia in subjects with symptomatic benign hyperplasia (BPH). Primary effectiveness will be achieved by looking at the Quality of Recovery Visual...

What is the current status of trial NCT01876706?

This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2013-04. Estimated completion is 2018-09-04.

What interventions are being tested in trial NCT01876706?

The interventions under investigation include: UroLift® System (DEVICE).

Who is sponsoring clinical trial NCT01876706?

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

How this trial's enrollment target compares

Where NCT01876706's enrollment target sits among peer trials

51 1279th of 2000 higher than 722 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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Source: ClinicalTrials.gov NCT01876706, the US trial registry maintained by the National Library of Medicine. NCT01876706 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.