Regional AnesthesiaBlockbaseNCT06460792
Ultrasound-guided Peripheral Nerve Blocks - a Database
An observational study of Regional Anesthesia, run by Nordsjaellands Hospital at 1 site in Denmark.
Trial 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. Read more about this study
- Who is it for?
- Ages 2 years and older
- Conditions the study is for
- Regional Anesthesia
- What is being tested?
- Ultrasound-guided peripheral nerve block
- Type of treatment
- Surgery or procedure
- How many people
- 5,000 participants
- Where
- 1 siteDenmark
- Study dates
- 4 Jun 2024to 4 Jun 2029
- How long will I take part?
- 5 Years
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 2 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Patients treated with a peripheral nerve block as part of their normal treatment
Who may be able to join
- age > 2 years
Who cannot join
- Infection at puncture site
- Allergy to local anesthetics
- Unable to understand given oral instruction
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Christoffer Jørgensen, MD contact
Denmark1 site, 1 recruiting
- Recruiting
Dept of Anesthesiology, Nordsjællands Hospital
Hillerød, 3400
Kai Lange, MD
About this study
Official title: The Quality of Ultrasound-guided Peripheral Nerve Blocks, Nerve Injury, Bleeding Complications and Learning - a Prospective Observational Cohort Study
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.
Read the detailed description
Introduction 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. These three points are described in more detail below:
- 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.
- 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.
- 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
- Regional Anesthesia
- Being tested
- Ultrasound-guided peripheral nerve block
- Keywords
- nerve block, ultrasound guidance, complications, nerve injury, bleeding, success rate, learning
- Medical subject headings
- Hemorrhage
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Ultrasound-guided peripheral nerve blockProcedure or surgery
Ultrasound-guided peripheral nerve blocks. Registration of quality, complications and learning as detailed in the description
What is being measured
The primary outcome is the main question the study is designed to answer.
Block Success
Clinical evaluation of nerve function
Measured: 2 hours
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Jun 2024
- Study start4 Jun 2024
- Primary completion4 Jun 2029 (estimated)
- Study completion4 Jun 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Regional AnesthesiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 5,000 participants (estimated)
- Target duration
- 5 Years
Sponsor and investigators
- Lead sponsor
- Nordsjaellands Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Christian Rothe, MD, Principal investigator, Nordsjællands Hospital Hillerød
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06460792
- Sponsor's protocol ID
- p-2024-15805
- Acronym
- Blockbase
- Status last verified
- Jun 2024
- First submitted
- 4 Jun 2024
- Last updated
- 14 Jun 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 14 Jun 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Quality of Ultrasound-guided Peripheral Nerve Blocks, Nerve Injury, Bleeding Complications and Learning - a Prospective Observational Cohort Study
- ClinicalTrials.gov ID
- NCT06460792
- Acronym / sponsor ID
- Blockbase / p-2024-15805
- Conditions
- Regional Anesthesia
- Keywords
- nerve block, ultrasound guidance, complications, nerve injury, bleeding, success rate, learning
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 5,000 participants (estimated)
- Lead sponsor
- Nordsjaellands HospitalUniversity, hospital or other
- Study start
- 4 Jun 2024 (actual)
- Primary completion
- 4 Jun 2029 (estimated)
- Study completion
- 4 Jun 2029 (estimated)
- First posted
- 14 Jun 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Introduction 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. These three points are described in more detail below:
- 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.
- 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.
- 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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 5 Years
Who may qualify
- Ages
- 2 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Patients treated with a peripheral nerve block as part of their normal treatment
Key inclusion criteria (1 listed)
- age > 2 years
Key exclusion criteria (3 listed)
- Infection at puncture site
- Allergy to local anesthetics
- Unable to understand given oral instruction
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Ultrasound-guided peripheral nerve blockUltrasound-guided peripheral nerve blocks. Registration of quality, complications and learning as detailed in the description | Procedure or surgery | – |
Primary outcome
Block Success
Time frame: 2 hours
Clinical evaluation of nerve function
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Jun 2024.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Christoffer Jørgensen, MD contact
Christian Rothe, MD principal investigator
Nordsjællands Hospital Hillerød
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Regional Anesthesia, run by Nordsjaellands Hospital at 1 site in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 14 Jun 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Kai Lange, MD (+4548294252, kai.henrik.wiborg.lange@regionh.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Block Success (time frame: 2 hours). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jun 2024.