Pain Relief in Premature Newborns Through Maternal Intervention During Venipuncture
Recruiting
N/A
Interventional Study
Premature Newborns
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 32 Weeks – 34 Weeks
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 48 (estimated)
- Sponsor
- University Hospital, Strasbourg, France · Other
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About This Trial
Extremely premature newborn infants (ELNs) admitted to hospital are exposed to stressful and painful stimuli, and often to maternal separation, which can affect their long-term neurological development. Child- and family-centred developmental care (CFDC) in neonatology aims to adapt the hospital environment to the needs of the child, support the continued presence of the family and help to improve…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Very premature babies born before the gestational age (GA) of 32 weeks of amenorrhoea (SA) whose corrected age (CA) does not exceed 34 SA at the time of their participation.
* NN requiring close biological monitoring by a PV.
* Hospitalised in the NN medicine and intensive car…
Contacts