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NCT06653595: PAP-LM

Breastfeeding Support and Promotion Program to Improve the Health of Premature Babies (PAP-LM)

Completed NA Last updated 22 October 2024
What this trial tests

NA trial testing Programme to Support Breastfeeding in Prematurity; Extreme in 162 participants. Completed in 20 March 2024.

Timeline
13 October 2021
Primary endpoint
15 February 2024
20 March 2024

Quick facts

Lead sponsorUniversity of Barcelona
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment162
Start date13 October 2021
Primary completion15 February 2024
Estimated completion20 March 2024
Sites2 locations across Spain

Drugs / interventions tested

Conditions studied

Sponsor

University of Barcelona

Who can join

18 and older, female only, with Prematurity; Extreme or Prematurity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study evaluates the effectiveness of a breastfeeding support and promotion program to increase exclusive breastfeeding rates in the preterm group. The intervention is performed by an Advanced Practice Nurse and International Board Certified Breastfeeding Consultant (IBCLC), with high expertise in breastfeeding problems. It is a combination of face-to-face, home care and telephone attention to improve the adherence to breastfeeding. The intervention lasts 6 months.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Prematurity; Extreme

Currently open trials in the same condition.

Other University of Barcelona trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06653595.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing