drugset / Trial / NCT06668116

The Impact of Local Anesthetic Dilution on Possible Blinding for Nerve Blocks

NCT06668116 ↗

Completed 17 enrolled Balgrist University Hospital
RandomizedCrossoverDouble-blindOther

Summary

This study aims to determine the appropriate dosage of a placebo anesthetic to enable future placebo-controlled studies that can more accurately examine the effects of nerve blocks. The main challenge in conducting such studies is the difficulty in blinding participants and researchers due to the noticeable effects of nerve blocks, such as numbness and motor impairments. The goal is to find a placebo solution that can: * Mimic the sensations of a real nerve block * Not provide actual pain relief * Allow for effective blinding in future studies By developing an appropriate placebo, researchers hope to: * Enable more rigorous investigations into the efficacy of nerve blocks for pain management * Conduct comprehensive placebo-controlled studies, which are currently lacking in the field * Overcome the obstacle of ensuring successful blinding in nerve block research This study is focused to establish a methodology for creating a convincing placebo that can be used in future research to more accurately assess the true effects of nerve blocks in pain medicine.

Timeline

Start
2024-12-11
Primary completion
2025-10-31
Completion
2025-10-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropivacaine Other / unclassified 0.1 % —
Subject Ropivacaine Other / unclassified 0.5 % —

Indications

No indication recorded.