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Search / Trial NCT06668116

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

Launched by BALGRIST UNIVERSITY HOSPITAL · Oct 30, 2024

Trial Information

Current as of August 21, 2025

Recruiting

Keywords

Peripheral Nerve Blocks Placebo Controlled Studies Blinding In Clinical Trials

ClinConnect Summary

This clinical trial is looking to find the right dosage of a placebo anesthetic that can help researchers better study nerve blocks, which are used for pain management. The goal is to create a fake treatment that feels similar to a real nerve block—meaning it might cause numbness—but doesn't actually relieve pain. This is important because it will help ensure that both participants and researchers don’t know who is receiving the real treatment and who is getting the placebo in future studies. By achieving this, researchers can more accurately understand how effective nerve blocks are.

If you’re between the ages of 18 and 64 and are generally healthy, you may be eligible to participate in this study. However, there are certain conditions that could exclude you, such as allergies to specific anesthetics, any current pain issues, or a history of certain medical conditions. Participants will be asked to provide written consent and can expect to help shape future pain management research by contributing to the development of this placebo. Overall, this trial aims to improve our understanding of how nerve blocks work and their effectiveness in treating pain.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • ASA I - II, both sexes
  • ≥ 18 years old
  • \< 65 years old
  • Written informed consent as documented by signature
  • Exclusion Criteria:
  • Known allergy or hypersensitivity to a ropivacaine, amide local anesthetics or ultrasound gel
  • Any history of chronic or acute pain at the moment of enrollment into the study
  • Treatment with any substance having a relation to pain or pain modulation (antidepressants, opioids, benzodiazepines, anticonvulsants)
  • Intake of any analgesic 48 hours prior to the conduction of any of the study stages
  • Severe coagulopathy
  • History of cardiovascular disease
  • History of alcohol abuse or the intake of psychotropic drugs
  • Pregnancy, ruled out by history
  • Infection at the injection site or a systemic infection
  • Fever of unknown origin
  • Motor or sensory abnormalities in the arm
  • Previous enrollment into the current study

About Balgrist University Hospital

Balgrist University Hospital is a leading academic medical center based in Zurich, Switzerland, renowned for its expertise in musculoskeletal health and rehabilitation. As a prominent sponsor of clinical trials, the hospital is dedicated to advancing medical research and improving patient outcomes through innovative studies in orthopedics, neurology, and rehabilitation sciences. With a strong commitment to interdisciplinary collaboration and patient-centered care, Balgrist University Hospital leverages its state-of-the-art facilities and a team of experienced researchers to drive clinical advancements and foster the translation of scientific discoveries into practical therapies.

Locations

Zurich, , Switzerland

Patients applied

0 patients applied

Trial Officials

Hagen Bomberg, Medical Doctor

Principal Investigator

Deputy Head of Anesthesiology

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported