Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

Gastric Emptying After a Yoghurt Breakfast in Children: a Pilot Study

Children are asked to fast before anaesthesia to reduce the amount of material remaining in the stomach. Prolonged fasting can cause hunger, thirst and discomfort. Although shorter fasting intervals have been introduced for clear fluids and breast milk, less is known about how quickly a light yoghurt breakfast leaves the stomach. Yoghurt differs from clear fluids in its nutrient content and semi-solid consistency. The primary aim of this study is to compare gastric emptying after three versus four hours of fasting following yoghurt intake in 24 children aged 1 to 10 years undergoing elective upper gastrointestinal endoscopy under anaesthesia at Baskent University Faculty of Medicine Ankara Hospital. Children will be randomly allocated to two equal groups. They may eat yoghurt freely up to a maximum of 150 g; there is no prescribed fixed or weight-based dose, and the amount actually eaten will be recorded. Ultrasound will assess stomach contents at the assigned fasting interval. If the stomach has not emptied according to the study criterion, the assessment will be repeated at 10-minute intervals before proceeding with anaesthesia. Gastric contents will also be assessed directly during endoscopy. The clinicians performing ultrasound and endoscopy will not know the assigned group; the anaesthetist will know it. The primary outcome is the proportion of children with an empty stomach at the first ultrasound assessment, compared between the three-hour and four-hour groups. The primary hypothesis is that a three-hour interval after yoghurt intake will yield a similar proportion of empty stomachs to a four-hour interval. Secondary outcomes include estimated gastric volume, endoscopic findings, hunger, and agreement between ultrasound and endoscopic assessment.

Participants needed: 24
Trial details
Age: 1-10Biological sex: AllType: InterventionalSponsor: Baskent University Ankara HospitalUpdated: Oct 8, 2026Locations: 1
Eligibility criteria

Age 1 to 10 years. [+3]

Cardiac disease or dysfunction. [+4]

Status: Recruiting

Impact of Standardized Skin-to-Skin Care on Clinical Outcomes in Infants Born ≤ 32 Weeks: A Multicenter Study

This study is a multi-center, prospective pre-post clinical study conducted under the leadership of the Turkish Neonatal Society. It aims to investigate the effects of a standardized skin-to-skin care in NICU, initiated early and applied regularly, on recieving exclusive mothers' milk at discharge and clinical outcomes for preterm infants born ≤ 32 weeks of gestation. 1. Primary Objective: To evaluate the rate of receiving exclusive mothers' milk at discharge for infants born ≤ 32 weeks of gestation who have received skin-to-skin care in accordance with the study protocol. 2. Secondary Objective: To evaluate the rates of neonatal sepsis, intraventricular hemorrhage, and necrotizing enterocolitis (stage 2 and above) as well as the length of hospital stay for infants born at or below 32 weeks of gestation who have received skin-to-skin care in accordance with the study protocol.

Participants needed: 120
Trial details
Age: 1+Biological sex: AllType: InterventionalSponsor: Baskent University Ankara HospitalUpdated: Nov 4, 2024Locations: 1
Eligibility criteria

Infants born at gestational age ≤ 32 weeks

Death before NICU discharge [+1]

Status: Recruiting

Evaluation of the Frequency, Risk Factors, and Outcomes of ROP in Infants With a BW >1500 Grs or GA ≥33 Wks in Turkey.

The study includes preterm infants who are being screened for ROP between August 1,2023 and August 1, 2024 in 94 neonatal intensive care units (NICUs) in Turkey. Infants with birth weight (BW) of \>1500 g or ≥ 33 weeks' gestation who are screened for retinopathy of prematurity are included. The incidence of any ROP, severe ROP and treatment modalities will be determined. The risk factors for ROP development will also be evaluated.

Participants needed: 1,000
Trial details
Age: 28+Biological sex: AllType: ObservationalSponsor: Baskent University Ankara HospitalUpdated: Nov 1, 2024Locations: 1
Eligibility criteria

Infants with BW >1500 g or ≥33 weeks' gestation who were determined to be at ris...

Neonates who died before the first ROP examination are excluded from the study.