Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
5000 participants
OBSERVATIONAL
2024-06-04
2029-06-04
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Visualizing Peripheral Nerves Using Ultrasound-Guided Approach
NCT00221949
Ultrasound Guidance in Nerve Block Anaesthesia
NCT00213954
Saphenous Nerve Block for Foot and Ankle Surgery
NCT02382744
Ultrasound-guided Selective Blockade of the Saphenous and Obturator Nerves Following Total Knee Arthroplasty
NCT02465827
Randomized Controlled Trial of Ultrasound Guided Needle Placement Versus Nerve Stimulation for Coracoid Infraclavicular Brachial Plexus Block
NCT00326261
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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. These three points are described in more detail below:
1. Success rate (block quality) It is difficult to get an overview of the success rates of peripheral nerve blocks. Most studies focus on one specific nerve block, and the number of included patients is often low. In addition, the block procedure is performed by a few anaesthesiologists who are highly skilled in the specific procedure. By establishing a database, including the most used peripheral nerve blocks used in different settings, i.e., surgery, perioperative pain management, and painful procedures, and by including anaesthesiologists with varying levels of experience and expertise, it will be possible to get a more detailed picture of factors that are important for achieving high success rates.
2. Complications Nerve injury. Peripheral nerve blocks are generally considered safe to use with low complication rates. However, complications can be severe and result in permanent nerve injury. Therefore, it is essential to get an overview of block-related complications and factors associated with these complications. Different regions have specific characteristics, and complications probably follow a characteristic pattern. A database with sufficient data will allow us to detail essential factors for understanding how complications develop and turn into permanent injuries.
Bleeding. Today, many patients receive anticoagulant therapy. We will, therefore, collect data on bleeding complications associated with the block procedure.
3. Learning Ultrasound-guided peripheral nerve blocks require a certain amount of skill to deposit LA in the correct place. By gathering data on block quality from individual anaesthesiologists over time it will be possible to gain insight into learning curves and factors important for learning different block procedures.
Methods Study design: Observational prospective cohort study. Setting: Initially, a single-centre study at the Department of Anaesthesiology, North Zealand Hospital. We envision to include as many centres as possible in Denmark.
Participants: Patients scheduled for peripheral nerve blocks. Prior to collecting follow-up data, informed consent will be obtained from each participant through an automated and secure sms system.
Variables: The following variables are registered:
Patient demographics: Social security number, age, sex, height, weight, comorbidity (diabetes, use of insulin, chronic pain, pain medication, anticoagulant medication), ASA status, and type of surgery performed.
Technical block data: Date and time for the peripheral nerve block, performing anaesthesiologist, block details (name of block, type of LA, volume of LA, concentration of LA, anatomical location of LA injection, adjuvants used, onset time).
Peripheral nerve block quality and success rate: success rate, need of supplementary blocks, use of tourniquet, reasons for block deemed unsuccessful.
Bleeding complications: details on bleeding complications associated with the block procedure.
Follow-up by surveys:
Day 1: duration of peripheral nerve block, pain after block termination. Day 2: measures if block duration \> 24 h. Day 30: signs of nerve injury: altered sensation, pain, decreased muscle force. Day 90: continuous signs of nerve injury: altered sensation, pain, decreased muscle force.
Day 365: continuous signs of nerve injury: altered sensation, pain, decreased muscle force.
Data sources/measurements: All variables are part of data that are normally registered for patients who have a peripheral nerve block. However, the purpose of establishing the database is to perform a systematic data capture. We will use the secure web application for online research databases, REDCap to enter data through electronic CRFs and through surveys sent to the patients (follow-up).
Study size: The purpose of establishing the database is to continuously register peripheral nerve blocks in patients. As such there is no pre-defined study size.
Statistical methods: We will use descriptive statistics and inferential statistical analyses, e.g., regression analyses, etc.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Ultrasound-guided peripheral nerve block
Ultrasound-guided peripheral nerve blocks. Registration of quality, complications and learning as detailed in the description
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Allergy to local anesthetics
* Unable to understand given oral instruction
2 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Nordsjaellands Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Christian Rothe, MD
Role: PRINCIPAL_INVESTIGATOR
Nordsjællands Hospital Hillerød
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Dept of Anesthesiology, Nordsjællands Hospital
Hillerød, , Denmark
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Kai Lange, MD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
p-2024-15805
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.