Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

The Impact of Masseter Muscle Thickness on the Feeding Process in Preterm Infants in Ultrasound Assessment

The aim of this study is to assess masseter muscle thickness using ultrasounds during oral feeding process in premature infants with gestational age from 28+0/7 to 32+0/7 weeks, taking into account the qualitative and quantitative aspects of oral feeding. The main question it aims to answer is: Does the thickness of the masseter muscle influence the course of development of the feeding function in premature newborns? The study will assess the influence of masseter muscle thickness on the oral feeding process in premature infants, which has significant cognitive value due to the dynamic development of feeding function in this group of newborns. Transitioning from enteral feeding via a nasogastric tube to full oral feeding is a crucial stage in the development of one of the most fundamental life functions - nutrition. Complete, effective, and safe oral feeding is also a factor in determining a newborn's discharge from the hospital. Research in the area of feeding is an important and ongoing goal for improving neonatal care in neonatal units. Furthermore, this study will provide preliminary data on masseter muscle thickness in premature infants, which may serve as a basis for further research.

Participants needed: 30
Trial details
Age: 28-32Biological sex: AllType: ObservationalSponsor: Polish Mother Memorial Hospital Research InstituteUpdated: Jun 18, 2026Duration: 4 Months
Eligibility criteria

28+0/7-32+0/7 weeks of gestational age; [+3]

newborns with defects that may significantly affect the development of feeding f... [+8]

Status: Not yet recruiting

Use of Intranasal Midazolam to Reduce Stress and Procedural Pain in Premature Infants During Routine ROP Examination.

The goal of this study is to learn about the safety and effectiveness of intranasal midazolam in newborns and infants born prematurely, undergoing Retinopathy of Prematurity (ROP) screening. The main question it aims to answer is: • Does use of intranasal midazolam is a safe, quick, non-invasive medication, that reduces the pain, stress, discomfort, and other complications in patients undergoing ROP screening? Researchers will compare the intervention group with a comparison group of the patients who will receive routine comfort care.

Participants needed: 40
Trial details
Phase: Phase 1Age: Up to 30Biological sex: AllType: InterventionalSponsor: Polish Mother Memorial Hospital Research InstituteUpdated: Mar 21, 2025Locations: 1
Eligibility criteria

Obtaining informed consent from a parent/legal guardian.

Newborns/infants not qualified for screening ophthalmologic examination (ROP). [+3]

Status: Recruiting

PMMHRI-Pitavastatin Registry

The PMMHRI-Pitavastatin Registry is a non-interventional, single-center registry conducted at the Polish Mother's Memorial Hospital Research Institute (PMMHRI). Established in January 2024, the registry enrolls all patients from the Department of Cardiology and Adult Congenital Heart Diseases, the Department of Endocrinology, as well as outpatient cardiology and endocrinology clinics who are prescribed pitavastatin.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Polish Mother Memorial Hospital Research InstituteUpdated: Mar 5, 2025Locations: 1
Eligibility criteria

patient takling pitavastatin based on the 2021 Polish Lipid Guidelines

Status: Recruiting

The Prevalence of Hyper-Lp(a)-Emia in the PMMHRI-Lp(a) Registry

The PMMHRI-Lp(a)-Registry is a non-interventional, single-center registry conducted in the Polish Mother's Memorial Hospital Research Institute (PMMHRI). The PMMHRI-Lp(a)-Registry was established in January 2022. Since then, all consecutive patients of the Department of Cardiology and Adult Congenital Heart Diseases, Department of Endocrinology, and outpatient cardiology and endocrinology clinics with the measured Lp(a) concentration have been included.

Participants needed: 2,000
Trial details
Biological sex: AllType: ObservationalSponsor: Polish Mother Memorial Hospital Research InstituteUpdated: Sep 24, 2024Locations: 1
Eligibility criteria

measured lipoprotein(a) concentration

Status: Recruiting

PMMHRI - Familial Hypercholesterolemia Registry

The registry is maintained at the Regional Centre for Rare Diseases, established in 2016, within Polish Mother's Memorial Hospital Research Institute. This facility diagnoses and treats over 80 distinct rare diseases in patients from across the country, including those with phenotypically or genetically confirmed familial hypercholesterolemia (FH).

Participants needed: 300
Trial details
Age: 1+Biological sex: AllType: ObservationalSponsor: Polish Mother Memorial Hospital Research InstituteUpdated: Aug 26, 2024Locations: 1Duration: 1 Year
Eligibility criteria

FH diagnosis