drugset / Trial / NCT05579509

Personalizing Preprocedural Sedation for Regional Anesthesia

NCT05579509

Phase 0 Completed 82 enrolled Brigham and Women's Hospital
RandomizedParallel-groupSingle-blindSupportive care

Summary

This is a prospective, randomized study in patients who receive a nerve block prior to surgery. The aim is to investigate whether individual differences in psychosocial and pain profiles may play a role in how patients experience sedation for regional anesthesia. The study will utilize a mixed-methods approach, including a randomized controlled intervention and semi-structured interviews, in order to systematically investigate the relationship between an individual patient's level of catastrophizing and efficacy of procedural sedation, while exploring patient satisfaction with the preoperative nerve block experience.

Timeline

Start
2022-10-22
Primary completion
2024-05-24
Completion
2024-05-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Fentanyl Other / unclassified Intravenous
Subject Midazolam Small molecule Intravenous

Indications

No indication recorded.