Nerve BlockBlock-aidNCT07849049
Training Non-Anesthesia Personnel to Perform Nerve Blocks in Microgravity
A study testing Simulated microgravity and Normal earth gravity in people with Nerve Block and Regional Anesthesia, run by Nova Scotia Health Authority at 1 site in Canada.
Trial summary
Space exploration is rapidly progressing with multiple upcoming missions planned to the moon and International Space Station, and projected missions to Mars in the early 2030s. Multiple types of injuries and surgical emergencies are possible during space travel. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Nerve Block, Regional Anesthesia, Microgravity
- What is being tested?
- Simulated microgravity and Normal earth gravity
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 siteCanada
- Study dates
- 20 Mar 2026to 29 Mar 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- adult (age >18 years)
- certified scuba divers
- no prior nerve block technique training.
- staff anesthesiologists or senior residents
- certified scuba divers
Who cannot join
- active ear nose and throat conditions that prevent ear equalization
- neuromotor conditions interfering with fine motor skills
- pregnancy
- inability to consent
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Training Non-Anesthesia Personnel to Perform Nerve Blocks in Microgravity: A Prospective Cohort Study
Space exploration is rapidly progressing with multiple upcoming missions planned to the moon and International Space Station, and projected missions to Mars in the early 2030s. Multiple types of injuries and surgical emergencies are possible during space travel. With the rapidly increasing number of travelers, healthcare providers need to refine our plans for responding to surgical emergencies in space.
It may not be possible to return injured crew members to earth for medical treatment depending on distance from earth and the severity of the injury. Furthermore, the casualty's physiologic changes in microgravity, and logistical limitations of repatriation make addressing medical emergencies challenging. Pain medications and general anesthesia have side effects that can impact safety in space and have worse side effect profiles when compared to on earth.
Read more
Regional anesthesia, injecting local anesthetic near to a nerve(s) to create a large area of numbness on the body, has been used for many years for pain management and to allow for surgery in remote settings on earth. Military personnel have used these techniques to provide effective pain control for evacuating wounded soldiers, while maintaining their cognition. For these reasons, regional anesthesia (aka 'nerve block') has been promoted as a viable solution for injured astronauts.
Our team has demonstrated that simple nerve blocks are possible in simulated microgravity among trained anesthesia providers. Recognizing that non-physician medical technicians may be integral to future space missions, this study aims to ascertain the feasibility of training such personnel to perform simple nerve blocks in microgravity.
Read the detailed description
With the burgeoning human presence in space, the need to prepare for medical emergencies in microgravity environments becomes increasingly critical. Space is an inherently hazardous environment, with 21 known fatalities. Most injuries occur during lift off or re-entry, but in-flight incidents have also been reported, including fires, blunt injuries, vehicular collisions, and loss of environmental controls. Extraction times vary significantly, with the potential for hours in low-earth orbit (LEO), days from the Moon, and months from Mars. In this case or during more distant space exploration, damage control procedures may be necessary.
If astronauts are injured, physiologic and logistic complexities necessitate a different approach from hospital-based care on Earth. In addition, due to ergonomic challenges of microgravity. Systemic pain medication is not optimal in that it can cause sedation, confusion, and even delirium. This could compromise safety for the crew given the small numbers of personnel who play critical roles. If a surgical intervention was required, general anesthesia is problematic for multiple reasons.
The benefits of regional anesthesia (nerve blocks) have been recognized in remote settings, including regions with fewer resources and trained providers. Regional anesthesia limits airway management, ventilation, and hemodynamic changes. The equipment is portable, offers stable hemodynamics, effective analgesia, minimal need for supplemental oxygen, and improved alertness. As each crew member's role is pivotal for mission success, regional anesthesia ensures their cognitive participation. Our group has shown that nerve blocks are feasible in a simulated microgravity environment when performed by anesthesiologists and anesthesia residents.
In specialized teams such as astronauts, rigorously trained for space exploration, there might not be the depth of personnel to allow physicians on crews. At the current time, most missions have a single Crew Medical Officer (CMO) who is usually not a physician. Space travel with its associated communication and logistical delays further emphasizes the need for such medical training so they can act without real-time guidance.
Aim Recognizing that non-physician medical technicians may be integral to future space missions, our study aims to ascertain the feasibility of training such personnel to perform simple nerve blocks in microgravity.
Hypothesis The investigators hypothesize that despite training about nerve block mechanics and ultrasound imaging, non-physician personnel have worse accuracy, time to injection, and ease of needle placement in a simulated microgravity environment than compared to normal gravity conditions. Furthermore, the investigators hypothesize that accuracy, time to injection, and ease of needle placement will be inferior to anesthesia providers in a simulated microgravity environment.
Methods This will be a prospective cohort study using within- and between-subjects comparisons. This study will assess the ease and success of ultrasound-guided injections ("nerve blocks") by non-anesthesia personnel comparing normal gravity to microgravity conditions using a meat model. Secondly, the ease and success rate of non-anesthesia participants will be compared to anesthesia participants.
Recruitment and Allocation The investigators will recruit 20 non-anesthesia military personnel and 5 anesthesia providers who are trained scuba divers. Inclusion criteria for the non-anesthesia group would be adult (age >18 years) certified scuba divers and those who have not had prior nerve block technique training. Inclusion criteria for the anesthesia group are that they are staff anesthesiologists or senior residents and certified scuba divers since nerve block training is part of basic anesthesia training.
Training session Recruited participants would be given a 4-hour training session on ultrasound imaging theory and practical optimization, needle visualization and control, basics of local anesthetics, basic sono-anatomy, and complications of nerve blocks. This session will be developed and led by regional anesthesia fellowship trained team members. There will be opportunities to practice image acquisition and needle placement with feedback. This session will take place the day before the study.
Meat model creation All injections will use a meat model. This meat model using beef muscle, beef tendon, and ballistics gel has been previously validated for accessing accuracy of US-guided injections.
Gravity conditions In the normal gravity condition, participants will be in a seated position with the meat model positioned in the chest wall of a mannikin, supported on a table. The ultrasound, phone, and dive case will be the same as in the microgravity condition. Participants will use hand signals to communicate with their block assistant since verbal communication will not be possible underwater.
In the microgravity condition, the participants will be scuba diving in a pool. The mannikin will be secured to a table at the bottom of the pool and they will empty their buoyancy control device (causing them to sink), effectively removing the added complexity of buoyancy control. An investigator will assist each participant with the block by positioning the meat model in the mannikin, passing equipment, and injecting the dye through a syringe once they are signalled to do so. However, the investigator will not give the participant guidance on the accuracy of the needle position or the quality of their ultrasound image.
Statistical analysis and power calculation Demographics will be collected (age, gender, prior medical training, experience with nerve blocks) and reported in aggregate for the purposes of external validity and generalizability. Outcomes will be compared between normal gravity and microgravity for non-anesthesia participants (within subjects, paired data). Outcomes will also be compared between anesthesia and non-anesthesia participants (between subjects, independent data).
Data will be analyzed using generalized estimating equations to adjust for the clustered nature of the data (i.e., blocks nested within participants). For binary outcomes (success vs. failure), a binomial outcome with a logit link will be used. For numerical outcomes, a normal distribution will be assumed, though loglinear models for skewed distributions will also be explored if they fit the data better.
Power analyses adjust sample sizes for the clustered design using the design effect method described by Bland (2004). Moreover, the design assumes 14 blocks per participant. The first a-priori power analysis is for comparing normal gravity and microgravity for non-anesthesia participants with the outcome of success vs. failure. Assuming a one-tailed alpha of 0.05, power of 80%, a normal gravity success rate of 90% and a microgravity success rate of 70%, and an intraclass correlation of 0.10, a total of 19 non-anesthesia participants will be required.
The second a-priori power analysis is for comparing normal gravity and microgravity for non-anesthesia participants for time to block, which has been used as a measure of ease in learning curve studies. Assuming a one-tailed alpha of 0.05, power of 80%, a mean difference of 12 seconds, a standard deviation of 23 seconds (based on data from our prior study), and an intraclass correlation of 0.10, a total of 15 participants will be needed.
- Conditions
- Nerve Block, Regional Anesthesia, Microgravity, Space Analogue
- Being tested
- Simulated microgravity, Normal earth gravity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Simulated microgravityOther
Neutral buoyancy underwater
Normal earth gravityOther
Same procedure on land
| Study group | Role | What they receive |
|---|---|---|
| Simulated Microgravity | Experimental | In the microgravity condition, the participants will be scuba diving in a pool. The mannikin will be secured to a table at the bottom of the pool and they will empty their buoyancy control device (causing them to sink), effectively removing the added complexity of buoyancy control. An investigator will assist each participant with the block by positioning the meat model in the mannikin, passing equipment, and injecting the dye through a syringe once they are signaled to do so. However, the investigator will not give the participant guidance on the accuracy of the needle position or the quality of their ultrasound image. Receives: Other: Simulated microgravity |
| Normal gravity | Active comparator | In the normal gravity condition, participants will be in a seated position with the meat model positioned in the chest wall of a mannikin, supported on a table. Participants will use a high-frequency (4-13 MHz) linear transducer and a 22G 50 mm echogenic needle to inject the meat model with 1-2 ml of water mixed with blue food coloring. The ultrasound, phone, and dive case will be the same as in the microgravity condition. Participants will use hand signals to communicate with their block assistant since verbal communication will not be possible underwater. Receives: Other: Normal earth gravity |
What is being measured
The primary outcome is the main question the study is designed to answer.
Injection success
Post-injection the models will be stored in a refrigerator for at least 24 hours to dry and allow the dye to settle. Two blinded investigators will dissect the models and score them. A successful nerve block will be defined as visible blue dye staining the outside of the beef tendon without evidence of injection inside of the tendon. The presence of primarily intraneural or intramuscular staining will be considered a failed block.
Measured: 3.5 minutes
Secondary outcomes (5)
Time to injection
Defined as the time from the transducer first touching the nerve block model to when the needle was removed from the model.
Time was censored at 3.5 minutes, such as the participants were signalled to stop at the maximum time and the attempt was recorded as incomplete (due to time constraints).
Measured: 3.5 minutes
Number of needle passes
Any needle passes that appeared to contact the tendon (simulated nerve), judged by noticeable movement of the tendon, were be recorded by the investigator. The number of needle passes were also recorded, judged as the number of times the needle was withdrawn and repositioned (adjustments in trajectory were not counted).
Measured: 3.5 minutes
Ease of ultrasound image acquisition
Scored immediately after each block in both conditions using a 5-point Likert scale (1 = very difficult, 2 = difficult, 3 = neutral, 4 = easy, 5 = very easy).
Measured: 5 minutes
Ease of needle placement
Scored immediately after each block in both conditions using a 5-point Likert scale (1 = very difficult, 2 = difficult, 3 = neutral, 4 = easy, 5 = very easy).
Measured: 5 minutes
Intraneural injection
Post-injection the models were be stored in a refrigerator for at least 24 hours to dry and allow the dye to settle. Two blinded investigators dissected the models to score the position of the dye. The presence of dye within the tendon will be considered an "intraneural" injection.
Measured: 3.5 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Sep 2026
- Study start20 Mar 2026
- Primary completion29 Mar 2026
- Study completion29 Mar 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (6)Papers the sponsor has linked to this study.
- Other trials for Nerve BlockStudies 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- This will be a prospective cohort study using within- and between-subjects comparisons. This study will assess the ease and success of ultrasound-guided injections ("nerve blocks") by non-anesthesia personnel comparing normal gravity to microgravity conditions using a meat model. Secondly, the ease and success rate of non-anesthesia participants will be compared to anesthesia participants.
- Masking
- None (open label)
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- Nova Scotia Health Authority
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Jon Bailey, Nova Scotia Health Authority
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07849049
- Sponsor's protocol ID
- REB # 2024-7417
- Acronym
- Block-aid
- Status last verified
- Sep 2026
- First submitted
- 17 Sep 2026
- Last updated
- 30 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: Ability to share would be based on ethical and Canadian Armed Forces approval on a case by case basis.
Publications
Kiberd MB, Brownbridge R, Mackin M, Werry D, Bird S, Barry G, Bailey JG. Feasibility of ultrasound-guided nerve blocks in simulated microgravity: a proof-of-concept study for regional anaesthesia during deep space missions. Br J Anaesth. 2024 Dec;133(6):1276-1283. doi: 10.1016/j.bja.2024.07.034. Epub 2024 Sep 25.
PubMed 39327151Brownbridge RG, Kiberd MB, Werry D, Bailey JG. Discriminative Ability of Dye Injected Into a Meat Model to Determine Accuracy of Ultrasound-Guided Injection. Simul Healthc. 2025 Feb 1;20(1):54-60. doi: 10.1097/SIH.0000000000000799. Epub 2024 Jun 10.
PubMed 38856652Komorowski M, Thierry S, Stark C, Sykes M, Hinkelbein J. On the Challenges of Anesthesia and Surgery during Interplanetary Spaceflight. Anesthesiology. 2021 Jul 1;135(1):155-163. doi: 10.1097/ALN.0000000000003789. No abstract available.
PubMed 33940633Scarpa J, Wu CL. The role for regional anesthesia in medical emergencies during deep space flight. Reg Anesth Pain Med. 2021 Oct;46(10):919-922. doi: 10.1136/rapm-2021-102710. Epub 2021 May 21.
PubMed 34021077Anderton R, Posselt B, Komorowski M, Hodkinson P. Medical considerations for a return to the Moon. Occup Med (Lond). 2019 Aug 22;69(5):311-313. doi: 10.1093/occmed/kqz099. No abstract available.
PubMed 31436819Komorowski M, Fleming S, Mawkin M, Hinkelbein J. Anaesthesia in austere environments: literature review and considerations for future space exploration missions. NPJ Microgravity. 2018 Feb 23;4:5. doi: 10.1038/s41526-018-0039-y. eCollection 2018.
PubMed 29507873
Study at a glance
From the registry record, last updated by the sponsor on 30 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Training Non-Anesthesia Personnel to Perform Nerve Blocks in Microgravity: A Prospective Cohort Study
- ClinicalTrials.gov ID
- NCT07849049
- Acronym / sponsor ID
- Block-aid / REB # 2024-7417
- Conditions
- Nerve Block, Regional Anesthesia, Microgravity, Space Analogue
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Nova Scotia Health AuthorityUniversity, hospital or other
- Study start
- 20 Mar 2026 (actual)
- Primary completion
- 29 Mar 2026 (actual)
- Study completion
- 29 Mar 2026 (actual)
- First posted
- 30 Sep 2026 (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.
Space exploration is rapidly progressing with multiple upcoming missions planned to the moon and International Space Station, and projected missions to Mars in the early 2030s. Multiple types of injuries and surgical emergencies are possible during space travel. With the rapidly increasing number of travelers, healthcare providers need to refine our plans for responding to surgical emergencies in space.
It may not be possible to return injured crew members to earth for medical treatment depending on distance from earth and the severity of the injury. Furthermore, the casualty's physiologic changes in microgravity, and logistical limitations of repatriation make addressing medical emergencies challenging. Pain medications and general anesthesia have side effects that can impact safety in space and have worse side effect profiles when compared to on earth.
Regional anesthesia, injecting local anesthetic near to a nerve(s) to create a large area of numbness on the body, has been used for many years for pain management and to allow for surgery in remote settings on earth. Military personnel have used these techniques to provide effective pain control for evacuating wounded soldiers, while maintaining their cognition. For these reasons, regional anesthesia (aka 'nerve block') has been promoted as a viable solution for injured astronauts.
Our team has demonstrated that simple nerve blocks are possible in simulated microgravity among trained anesthesia providers. Recognizing that non-physician medical technicians may be integral to future space missions, this study aims to ascertain the feasibility of training such personnel to perform simple nerve blocks in microgravity.
Detailed description
With the burgeoning human presence in space, the need to prepare for medical emergencies in microgravity environments becomes increasingly critical. Space is an inherently hazardous environment, with 21 known fatalities. Most injuries occur during lift off or re-entry, but in-flight incidents have also been reported, including fires, blunt injuries, vehicular collisions, and loss of environmental controls. Extraction times vary significantly, with the potential for hours in low-earth orbit (LEO), days from the Moon, and months from Mars. In this case or during more distant space exploration, damage control procedures may be necessary.
If astronauts are injured, physiologic and logistic complexities necessitate a different approach from hospital-based care on Earth. In addition, due to ergonomic challenges of microgravity. Systemic pain medication is not optimal in that it can cause sedation, confusion, and even delirium. This could compromise safety for the crew given the small numbers of personnel who play critical roles. If a surgical intervention was required, general anesthesia is problematic for multiple reasons.
The benefits of regional anesthesia (nerve blocks) have been recognized in remote settings, including regions with fewer resources and trained providers. Regional anesthesia limits airway management, ventilation, and hemodynamic changes. The equipment is portable, offers stable hemodynamics, effective analgesia, minimal need for supplemental oxygen, and improved alertness. As each crew member's role is pivotal for mission success, regional anesthesia ensures their cognitive participation. Our group has shown that nerve blocks are feasible in a simulated microgravity environment when performed by anesthesiologists and anesthesia residents.
In specialized teams such as astronauts, rigorously trained for space exploration, there might not be the depth of personnel to allow physicians on crews. At the current time, most missions have a single Crew Medical Officer (CMO) who is usually not a physician. Space travel with its associated communication and logistical delays further emphasizes the need for such medical training so they can act without real-time guidance.
Aim Recognizing that non-physician medical technicians may be integral to future space missions, our study aims to ascertain the feasibility of training such personnel to perform simple nerve blocks in microgravity.
Hypothesis The investigators hypothesize that despite training about nerve block mechanics and ultrasound imaging, non-physician personnel have worse accuracy, time to injection, and ease of needle placement in a simulated microgravity environment than compared to normal gravity conditions. Furthermore, the investigators hypothesize that accuracy, time to injection, and ease of needle placement will be inferior to anesthesia providers in a simulated microgravity environment.
Methods This will be a prospective cohort study using within- and between-subjects comparisons. This study will assess the ease and success of ultrasound-guided injections ("nerve blocks") by non-anesthesia personnel comparing normal gravity to microgravity conditions using a meat model. Secondly, the ease and success rate of non-anesthesia participants will be compared to anesthesia participants.
Recruitment and Allocation The investigators will recruit 20 non-anesthesia military personnel and 5 anesthesia providers who are trained scuba divers. Inclusion criteria for the non-anesthesia group would be adult (age >18 years) certified scuba divers and those who have not had prior nerve block technique training. Inclusion criteria for the anesthesia group are that they are staff anesthesiologists or senior residents and certified scuba divers since nerve block training is part of basic anesthesia training.
Training session Recruited participants would be given a 4-hour training session on ultrasound imaging theory and practical optimization, needle visualization and control, basics of local anesthetics, basic sono-anatomy, and complications of nerve blocks. This session will be developed and led by regional anesthesia fellowship trained team members. There will be opportunities to practice image acquisition and needle placement with feedback. This session will take place the day before the study.
Meat model creation All injections will use a meat model. This meat model using beef muscle, beef tendon, and ballistics gel has been previously validated for accessing accuracy of US-guided injections.
Gravity conditions In the normal gravity condition, participants will be in a seated position with the meat model positioned in the chest wall of a mannikin, supported on a table. The ultrasound, phone, and dive case will be the same as in the microgravity condition. Participants will use hand signals to communicate with their block assistant since verbal communication will not be possible underwater.
In the microgravity condition, the participants will be scuba diving in a pool. The mannikin will be secured to a table at the bottom of the pool and they will empty their buoyancy control device (causing them to sink), effectively removing the added complexity of buoyancy control. An investigator will assist each participant with the block by positioning the meat model in the mannikin, passing equipment, and injecting the dye through a syringe once they are signalled to do so. However, the investigator will not give the participant guidance on the accuracy of the needle position or the quality of their ultrasound image.
Statistical analysis and power calculation Demographics will be collected (age, gender, prior medical training, experience with nerve blocks) and reported in aggregate for the purposes of external validity and generalizability. Outcomes will be compared between normal gravity and microgravity for non-anesthesia participants (within subjects, paired data). Outcomes will also be compared between anesthesia and non-anesthesia participants (between subjects, independent data).
Data will be analyzed using generalized estimating equations to adjust for the clustered nature of the data (i.e., blocks nested within participants). For binary outcomes (success vs. failure), a binomial outcome with a logit link will be used. For numerical outcomes, a normal distribution will be assumed, though loglinear models for skewed distributions will also be explored if they fit the data better.
Power analyses adjust sample sizes for the clustered design using the design effect method described by Bland (2004). Moreover, the design assumes 14 blocks per participant. The first a-priori power analysis is for comparing normal gravity and microgravity for non-anesthesia participants with the outcome of success vs. failure. Assuming a one-tailed alpha of 0.05, power of 80%, a normal gravity success rate of 90% and a microgravity success rate of 70%, and an intraclass correlation of 0.10, a total of 19 non-anesthesia participants will be required.
The second a-priori power analysis is for comparing normal gravity and microgravity for non-anesthesia participants for time to block, which has been used as a measure of ease in learning curve studies. Assuming a one-tailed alpha of 0.05, power of 80%, a mean difference of 12 seconds, a standard deviation of 23 seconds (based on data from our prior study), and an intraclass correlation of 0.10, a total of 15 participants will be needed.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- This will be a prospective cohort study using within- and between-subjects comparisons. This study will assess the ease and success of ultrasound-guided injections ("nerve blocks") by non-anesthesia personnel comparing normal gravity to microgravity conditions using a meat model. Secondly, the ease and success rate of non-anesthesia participants will be compared to anesthesia participants.
| Arm | Type | Receives |
|---|---|---|
| Simulated Microgravity | Experimental | Other: Simulated microgravityIn the microgravity condition, the participants will be scuba diving in a pool. The mannikin will be secured to a table at the bottom of the pool and they will empty their buoyancy control device (causing them to sink), effectively removing the added complexity of buoyancy control. An investigator will assist each participant with the block by positioning the meat model in the mannikin, passing equipment, and injecting the dye through a syringe once they are signaled to do so. However, the investigator will not give the participant guidance on the accuracy of the needle position or the quality of their ultrasound image. |
| Normal gravity | Active comparator | Other: Normal earth gravityIn the normal gravity condition, participants will be in a seated position with the meat model positioned in the chest wall of a mannikin, supported on a table. Participants will use a high-frequency (4-13 MHz) linear transducer and a 22G 50 mm echogenic needle to inject the meat model with 1-2 ml of water mixed with blue food coloring. The ultrasound, phone, and dive case will be the same as in the microgravity condition. Participants will use hand signals to communicate with their block assistant since verbal communication will not be possible underwater. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- adult (age >18 years)
- certified scuba divers
- no prior nerve block technique training.
- staff anesthesiologists or senior residents
- certified scuba divers
Key exclusion criteria (4 listed)
- active ear nose and throat conditions that prevent ear equalization
- neuromotor conditions interfering with fine motor skills
- pregnancy
- inability to consent
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 |
|---|---|---|
| Simulated microgravityNeutral buoyancy underwater | Other | Simulated Microgravity |
| Normal earth gravitySame procedure on land | Other | Normal gravity |
Primary outcome
Injection success
Time frame: 3.5 minutes
Post-injection the models will be stored in a refrigerator for at least 24 hours to dry and allow the dye to settle. Two blinded investigators will dissect the models and score them. A successful nerve block will be defined as visible blue dye staining the outside of the beef tendon without evidence of injection inside of the tendon. The presence of primarily intraneural or intramuscular staining will be considered a failed block.
5 secondary outcomes
Time to injection
Time frame: 3.5 minutes
Number of needle passes
Time frame: 3.5 minutes
Ease of ultrasound image acquisition
Time frame: 5 minutes
Ease of needle placement
Time frame: 5 minutes
Intraneural injection
Time frame: 3.5 minutes
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Sep 2026.
- Background: PubMed 39327151Kiberd MB, Brownbridge R, Mackin M, Werry D, Bird S, Barry G, Bailey JG. Feasibility of ultrasound-guided nerve blocks in simulated microgravity: a proof-of-concept study for regional anaesthesia during deep space missions. Br J Anaesth. 2024 Dec;133(6):1276-1283. doi: 10.1016/j.bja.2024.07.034. Epub 2024 Sep 25.
- Background: PubMed 38856652Brownbridge RG, Kiberd MB, Werry D, Bailey JG. Discriminative Ability of Dye Injected Into a Meat Model to Determine Accuracy of Ultrasound-Guided Injection. Simul Healthc. 2025 Feb 1;20(1):54-60. doi: 10.1097/SIH.0000000000000799. Epub 2024 Jun 10.
- Background: PubMed 33940633Komorowski M, Thierry S, Stark C, Sykes M, Hinkelbein J. On the Challenges of Anesthesia and Surgery during Interplanetary Spaceflight. Anesthesiology. 2021 Jul 1;135(1):155-163. doi: 10.1097/ALN.0000000000003789. No abstract available.
- Background: PubMed 34021077Scarpa J, Wu CL. The role for regional anesthesia in medical emergencies during deep space flight. Reg Anesth Pain Med. 2021 Oct;46(10):919-922. doi: 10.1136/rapm-2021-102710. Epub 2021 May 21.
- Background: PubMed 31436819Anderton R, Posselt B, Komorowski M, Hodkinson P. Medical considerations for a return to the Moon. Occup Med (Lond). 2019 Aug 22;69(5):311-313. doi: 10.1093/occmed/kqz099. No abstract available.
- Background: PubMed 29507873Komorowski M, Fleming S, Mawkin M, Hinkelbein J. Anaesthesia in austere environments: literature review and considerations for future space exploration missions. NPJ Microgravity. 2018 Feb 23;4:5. doi: 10.1038/s41526-018-0039-y. eCollection 2018.
- Individual participant dataSharing planned: Undecided. Ability to share would be based on ethical and Canadian Armed Forces approval on a case by case basis.
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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. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Simulated microgravity and Normal earth gravity in people with Nerve Block and Regional Anesthesia, run by Nova Scotia Health Authority at 1 site in Canada.
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 5 inclusion and 4 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: finished, as of the sponsor's last update on 30 Sep 2026. 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 Canada. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Injection success (time frame: 3.5 minutes). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07849049, which also lists 6 linked publications.
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 30 Sep 2026.