CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 90 enrolled
Drug / intervention
Phentolamine Mesylate 0.235 MG/ML [OraVerse]drug
Likely dose
Phentolamine Mesylate 0.235 MG/ML [OraVerse]from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03740386
NCT03740386N/ACompleted

Phentolamine Mesylate as a Reversal of Local Anesthesics

León Formación·interventional·Posted Nov 14, 2018·Updated Nov 14, 2018

In Brief

A clinical study evaluating Phentolamine Mesylate 0.235 MG/ML [OraVerse] for Anesthesia, Local. Completed, enrolled 90 participants.

Detailed Summary

Oraverse © (Phentolamine mesylate) is a product designed to reverse the effect of local anesthetics used in dentistry. Its main objective is to reduce the postoperative period during which the patient suffers from the lack of sensitivity in the perioral soft tissues, it is an obvious discomfort, a difficulty to speak or eat, and sometimes a risk of self-injury in the lips and / or tongue . The product was approved by the FDA in 2008 although the introduction in Spain has not occurred until December 2015. There are numerous studies that support its use, its effectiveness and safety, although none of the Spanish population, who have not yet had the opportunity to experience it.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedNov 14, 2018
Enrollment StartJan 1, 2016
Primary CompletionNov 9, 2018
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 7.6 years ago

Interventions

Phentolamine Mesylate 0.235 MG/ML [OraVerse]drug

compare effect of phentolamine mesylate in three arms