NCT06460792 Ultrasound-guided Peripheral Nerve Blocks - a Database
| NCT ID | NCT06460792 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Nordsjaellands Hospital |
| Condition | Regional Anesthesia |
| Study Type | OBSERVATIONAL |
| Enrollment | 5,000 participants |
| Start Date | 2024-06-04 |
| Primary Completion | 2029-06-04 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 5,000 participants in total. It began in 2024-06-04 with a primary completion date of 2029-06-04.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Peripheral nerve blocks are often used in anaesthesia. They can be used as the only method of anaesthesia during surgery or in combination with other methods, e.g., general anaesthesia and sedation. Moreover, peripheral nerve blocks are used to treat postoperative pain, alleviate pain in trauma patients, and for painful procedures. For a method to be clinically useful, it is essential to understand the factors contributing to high success rates. It is equally important to know the complications related to the method. Finally, it is essential to establish a robust learning system where the anesthesiologists can track their nerve block performance over time and compare it to high performers and general performance. Therefore, we aim to establish a prospective and ongoing database to gain insight into 1) Factors contributing to block quality, e.g., success rate and nerve block duration; 2) Frequencies and types of nerve injuries and bleeding complications associated with the block procedure; 3) Tracking of block performance by anaesthesiologists.
Eligibility Criteria
Inclusion Criteria: \- age \> 2 years Exclusion Criteria * Infection at puncture site * Allergy to local anesthetics * Unable to understand given oral instruction
Contact & Investigator
Christian Rothe, MD
PRINCIPAL INVESTIGATOR
Nordsjællands Hospital Hillerød
Frequently Asked Questions
Who can join the NCT06460792 clinical trial?
This trial is open to participants of all sexes, aged 2 Years or older, studying Regional Anesthesia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06460792 currently recruiting?
Yes, NCT06460792 is actively recruiting participants. Contact the research team at kai.henrik.wiborg.lange@regionh.dk for enrollment information.
Where is the NCT06460792 trial being conducted?
This trial is being conducted at Hillerød, Denmark.
Who is sponsoring the NCT06460792 clinical trial?
NCT06460792 is sponsored by Nordsjaellands Hospital. The principal investigator is Christian Rothe, MD at Nordsjællands Hospital Hillerød. The trial plans to enroll 5,000 participants.