Sticker sensors could make nerve blocks safer for kids
NCT ID NCT06982027
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study uses a non-invasive surface EMG device (sensor stickers on the skin) to measure how well regional anesthesia (nerve blocks) works during surgery in children and young adults up to age 21. The goal is to learn how to give nerve blocks more safely and effectively. Participants wear the stickers before, during, and after surgery. This is a research-only device, not yet approved for medical use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Sep 2025
- Expected to finish
-
Dec 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
0 to 21 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients ≤ 21 years of age * Patient presenting for a surgical procedure in which GA and a peripheral regional block will be used Exclusion Criteria: * Patients \> 21 years of age * Parent / patient refusal * Premature infants; neuromuscular disease; systemic infection; hemodynamic instability; coagulation disorder; degenerative CNS abnormality that precludes regional anesthesia; and local anesthetic allergy; pregnant women.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Surgery are added.
By submitting, you agree to our Terms of use
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Nationwide Children's Hospital
Columbus, Ohio, 43205, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can more phone calls after cancer surgery keep patients out of the hospital?
- Fixing broken ribs with surgery may cut pain better than drugs alone
- Ultrasound peers into Children's stomachs after Pre-Surgery drink
- Can Weight-Loss surgery patients skip the opioids?
- What stops surgeons from trying new techniques? 260 cancer surgeons asked
- Can IV nutrition at an outpatient clinic help malnourished surgery patients?