Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Effect of Music and Lighting on Anxiety During Urodynamic Study

This study is designed to evaluate the effects of environmental modifications, specifically music and lighting conditions, on anxiety in patients undergoing urodynamic study (UDS). Approximately 220 adult participants are planned to be randomly assigned to one of four intervention groups. Anxiety levels before and after the procedure will be assessed using the State-Trait Anxiety Inventory (STAI). The study aims to determine the independent and combined effects of music and lighting on patient anxiety during UDS.

Participants needed: 220
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Baskent University Ankara HospitalUpdated: Jul 14, 2026
Eligibility criteria

Adults aged 18 years or older. [+4]

Use of anxiolytic medications. [+5]

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.