Wireless MicroPremVitals Button Sensor in the NICU (NCT07732257) | Clinical Trial Compass
RecruitingNot Applicable
Wireless MicroPremVitals Button Sensor in the NICU
Canada10 participantsStarted 2026-06-19
Plain-language summary
A wireless and miniaturized vital sign (ECG, SpO2, Skin Temperature) sensor system, MicroPremVitals Button Sensors was developed by the Dr. John Rogers Laboratory (QSIB- Northwestern University, Chicago, USA) to facilitate vital sign monitoring in extremely preterm neonates.
Who can participate
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Infants admitted to the NICU with a gestational age of ≥ 22+0 weeks and ≤ 29+6 weeks at birth,
* AND \>72h of age at time of study,
* AND clinically stable,
* AND with the Neonatal Nurse Practitioner (i.e., NNP) and Healthcare Team in agreement for the patient to participate in the study.
Exclusion Criteria:
* Infants with a skin abnormality that would potentially increase the risk of injury,
* patient too unstable or family experiencing too much stress as determined by an attending physician or bedside care team to not be approached for recruitment.
* Infants admitted to the NICU with a gestational age of \< 22+0 weeks or \> 29+6 weeks at birth,
* and/or ≤ 72h of age at time of study,
* and/or not meeting all requirements of clinical stability,
* and/or with the Neonatal Nurse Practitioner (i.e., NNP)/Healthcare Team in disagreement for the patient to participate in the study.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
HR Accuracy
Timeframe: 6 months
2
Oxygen Saturation Accuracy
Timeframe: 6 months
3
Skin Temperature Accuracy
Timeframe: 6 months
Trial details
NCT IDNCT07732257
SponsorMcGill University Health Centre/Research Institute of the McGill University Health Centre