CompletedNot Applicable

Lateral Position MRI in Preterm Infants, an Observational Study

Italy22 participantsStarted 2023-02-16

Plain-language summary

The goal of this observational study is to evaluate safety of sedation in lateral position in premature babies undergone MRI. The main question it aims to answer are: * number of apneas during sedation * Maintenance of eupnea during deep sedation

Who can participate

Age range

50 Weeks

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: * \< 40 weeks Post Conceptional Age (PCA) Exclusion Criteria: * \> 50 weeks PCA * previous treatment with hypothermia for neonatal asphyxia * patients who received invasive positive pressure ventilation within the previous 48 h * preexisting cardiac arrhythmias * presence or suspicion of oncological pathology * neuromuscular or metabolic diseases * previous brain or abdominal surgery * presence of epicranial venous accesses * upper respiratory tract infections * refusal of informed consent by parents or inability to express it

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

Peripheral oxygen desaturation

Timeframe: Through study completion, an average of 7 month

Apnea

Timeframe: Through study completion, an average of 7 month

Trial details

NCT IDNCT05776238

SponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2023-09-30

View on ClinicalTrials.gov More Prematurity trials

Who can participate

Age range

50 Weeks

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.