NCT07849049

Brief 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. 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2026

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 20, 2026

Completed
9 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 29, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 29, 2026

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

September 17, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

September 30, 2026

Completed
Last Updated

September 30, 2026

Status Verified

September 1, 2026

Enrollment Period

9 days

First QC Date

September 17, 2026

Last Update Submit

September 25, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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.

    3.5 minutes

Secondary Outcomes (5)

  • Time to injection

    3.5 minutes

  • Number of needle passes

    3.5 minutes

  • Ease of ultrasound image acquisition

    5 minutes

  • Ease of needle placement

    5 minutes

  • Intraneural injection

    3.5 minutes

Study Arms (2)

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.

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.

Other: Normal earth gravity

Interventions

Neutral buoyancy underwater

Simulated Microgravity

Same procedure on land

Normal gravity

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • adult (age \>18 years)
  • certified scuba divers
  • no prior nerve block technique training.
  • staff anesthesiologists or senior residents
  • certified scuba divers

You may not qualify if:

  • active ear nose and throat conditions that prevent ear equalization
  • neuromotor conditions interfering with fine motor skills
  • pregnancy
  • inability to consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Survival Systems Training Limited

Dartmouth, Nova Scotia, B2Y 4K9, Canada

Location

Related Publications (6)

  • 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.

    PMID: 39327151BACKGROUND
  • Brownbridge 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.

    PMID: 38856652BACKGROUND
  • Komorowski 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.

    PMID: 33940633BACKGROUND
  • Scarpa 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.

    PMID: 34021077BACKGROUND
  • Anderton 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.

    PMID: 31436819BACKGROUND
  • Komorowski 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.

    PMID: 29507873BACKGROUND

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Model Details: 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.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Anesthesiologist

Study Record Dates

First Submitted

September 17, 2026

First Posted

September 30, 2026

Study Start

March 20, 2026

Primary Completion

March 29, 2026

Study Completion

March 29, 2026

Last Updated

September 30, 2026

Record last verified: 2026-09

Locations