drugset / Trial / NCT05912335

Clinical Efficiency of Xanthan Hydrogels Containing Local Anesthetics Encapsulated in Nanostructured Lipid Carries

NCT05912335

Phase 1 Completed 40 enrolled University of Campinas, Brazil
RandomizedCrossoverDouble-blindOther

Summary

In a crossover, randomized, placebo-controlled, double-blind study, 40 volunteers will receive the following formulations: hydrogels containing LAs (local anesthetic) - lidocaine and prilocaine (both at 2.5%) encapsulated in CLN (XAN-CLN) or not (XAN-CLN ), EMLA (topical anesthetic available on the market) and placebo hydrogel. The formulations will be applied for 2 minutes, bilaterally on the palatal mucosa (first premolar region), in two distinct sessions. Soon after removal of the topical formulation, an AL will be performed at the region using 0.3 mL of anesthetic solution at an injection speed of 1 mL/min. Pain resulting from needle insertion and LA injection will be measured using two visual analog scales (VAS).

Timeline

Start
2021-06-02
Primary completion
2022-02-20
Completion
2022-05-03

Drugs

EvaluationDrugModalityDoseRoute
Subject EMLA Unknown Topical
Subject Lidocaine Other / unclassified 2.5 % Topical
Subject prilocaine Small molecule 2.5 % Topical

Indications