CompletedNot Applicable

Prevention of Pain Caused by the Oro-gastric Tube Laying in Neonatology

France71 participantsStarted 2016-10-14

Plain-language summary

Subject of research : Evaluation of a technique of care to reduce the pain caused by the laying of the gastric tube in the newborn

Who can participate

Age range

2 Days – 14 Days

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: * Newborn term, or premature (from 32 weeks) from 48 hours to 14 days of life. * Presence of sucking reflex * Patient whose authors of parental authority have given their written consent for their participation * Patient affiliated to or benefiting from a social security scheme Exclusion Criteria: * Newborn intubated or NIV and / or sedated * Newborn with malformation (especially cleft palate) * Contra-indication to sugar administration * Newborn previously included in the study * Administration of analgesics in the previous 8 hours * Atresia of the unoperated esophagus * Non-operated oeso-tracheal fistula * Major swallowing disorders * Necrotizing ulcerative colitis

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

pain evaluation

Timeframe: Time of nurse care - thirty minutes maximum

Trial details

NCT IDNCT03142230

SponsorCentre Hospitalier Sud Francilien

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2018-08-13

View on ClinicalTrials.gov More Pain Score trials

Who can participate

Age range

2 Days – 14 Days

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.