← Back to Clinical Trials
Recruiting NCT06189352

NCT06189352 Positive Feeding of the Preterm Infant

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06189352
Status Recruiting
Phase
Sponsor Oslo Metropolitan University
Condition Preterm Infant
Study Type INTERVENTIONAL
Enrollment 15 participants
Start Date 2024-10-14
Primary Completion 2025-09

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Positive feeding of the preterm infant

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 15 participants in total. It began in 2024-10-14 with a primary completion date of 2025-09.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this feasibility study is to assess the feasibility to implement a feeding strategy for preterm infants. The main questions it aims to answer are: * Is it feasible to implement the PoP-intervention in a level 3a category Neonatal intensive care unit? * Is the PoP-intervention acceptable for parents of preterm infants and health care personnel working in Neonatal intensive care unit? Parents of preterm infants and health care personnel will be asked to follow a protocol of a feeding strategy based on the preterm infants development and cues throughout the NICU-stay.

Eligibility Criteria

Inclusion Criteria: * gestational age of 28 weeks * post menstrual age of 28 weeks after transition from regional hospital Exclusion Criteria: * diagnoses or malformations that makes eating difficult * triplets or more * parents not speaking/understanding Norwegian or English * parents with challenges or special needs for follow up

Contact & Investigator

Central Contact

Nina M Kyno, PhD

✉ ninam@oslomet.no

📞 +4790561929

Principal Investigator

Nina M Kyno, PhD

PRINCIPAL INVESTIGATOR

Oslo Metropolitan University

Frequently Asked Questions

Who can join the NCT06189352 clinical trial?

This trial is open to participants of all sexes, studying Preterm Infant. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06189352 currently recruiting?

Yes, NCT06189352 is actively recruiting participants. Contact the research team at ninam@oslomet.no for enrollment information.

Where is the NCT06189352 trial being conducted?

This trial is being conducted at Drammen, Norway.

Who is sponsoring the NCT06189352 clinical trial?

NCT06189352 is sponsored by Oslo Metropolitan University. The principal investigator is Nina M Kyno, PhD at Oslo Metropolitan University. The trial plans to enroll 15 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology