Database for Ultrasound-guided Peripheral Nerve Blocks
The Quality of Ultrasound-guided Peripheral Nerve Blocks, Nerve Injury, Bleeding Complications and Learning - a Prospective Observational Cohort Study
This study is creating a database to see how well ultrasound-guided nerve blocks work for anesthesia and to track any complications, helping doctors improve their skills and patient care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 5000 (estimated) |
| Ages | 2 Years and up |
| Sex | All |
| Sponsor | Nordsjaellands Hospital Academic / other |
| Locations | 1 site (Hillerød) |
| Trial ID | NCT06460792 on ClinicalTrials.gov |
What this trial studies
This study aims to establish a comprehensive database to analyze the effectiveness and complications of ultrasound-guided peripheral nerve blocks used in anesthesia. It will collect data on factors influencing block quality, such as success rates and duration, as well as the frequency and types of complications like nerve injuries and bleeding. The database will also allow anesthesiologists to track their performance over time and compare it with high-performing peers, ultimately enhancing the quality of care in regional anesthesia.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals over the age of 2 who require peripheral nerve blocks for anesthesia or pain management.
Not a fit: Patients with infections at the puncture site, allergies to local anesthetics, or those unable to understand oral instructions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the safety and effectiveness of peripheral nerve blocks, leading to better pain management for patients.
How similar studies have performed: Other studies have shown success in using databases to track anesthesia outcomes, making this approach both relevant and potentially impactful.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \- age \> 2 years Exclusion Criteria * Infection at puncture site * Allergy to local anesthetics * Unable to understand given oral instruction
Where this trial is running
Hillerød
- Dept of Anesthesiology, Nordsjællands Hospital — Hillerød, Denmark (Recruiting)
Study contacts
- Principal investigator: Christian Rothe, MD — Nordsjællands Hospital Hillerød
- Study coordinator: Kai Lange, MD
- Email: kai.henrik.wiborg.lange@regionh.dk
- Phone: +4548294252
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.