Mostrando 21 - 40 Resultados de 84 Para Buscar 'Blind Guardian', tiempo de consulta: 0.19s Limitar resultados
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    “…The randomization seed was generated using the time on the computer where the program was executed. BLINDING (MASKING): Participants, caregivers and study groups will be blinded to arm allocation. …”
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    por Choi, Hyun-Se, Cho, Seung-Hyun
    Publicado 2022
    “…Trial design: This study was a multicentre parallel randomised controlled, single-blind, trial conducted in three hospitals in Korea. …”
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  5. 25
    por Xia, Yong-Hua, Song, Yi-Ran
    Publicado 2016
    “…METHODS: A randomized, single-blind, controlled trial model was applied. The juvenile patients experiencing dental fear, whose parents or guardian had signed an informed consent form, were randomly divided into two groups. …”
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    “…METHODS AND ANALYSIS: ROPROP is an investigator-initiated, multicentre, placebo-controlled double-blind, randomised controlled trial aiming to assess the safety and efficacy of orally administered propranolol to reduce the risk of threshold ROP (stage 3) in extremely preterm infants at 48 weeks postmenstrual age (primary objective) and the rate of infants requiring local interventions for severe ROP (secondary objective). …”
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    “…SETTINGS AND DESIGN: Prospective, randomized, double-blind study. MATERIALS AND METHODS: After taking informed consent from the parents/guardian, 42 children aged 3–12 years who were scheduled to undergo unilateral upper limb surgeries below the elbow were randomized into two groups of 21 each. …”
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    “…DESIGN, SETTING, AND PARTICIPANTS: This randomized, double-blind, placebo-controlled phase 2 trial was conducted at a single tertiary pediatric intensive care unit from February 2016 to February 2019. …”
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    “…RESULTS: Eighty-eight questionnaires and satisfaction surveys were analyzed from 69 respondents (32 patients; 37 parents/guardians). Sixty-six (75.00%) surveys indicated satisfaction with the questionnaire. …”
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    “…Three patients (all in the 1500 mg/kg group) discontinued the study because of either physician decision/site Principal Investigator (PI) discretion, withdrawal by subject/patient/parent/guardian, or other non-safety reasons. In 5 patients who underwent serial lumbar punctures, HP-β-CD was detected in the CSF. …”
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  16. 36
    “…Chlamydia trachomatis (Ct) can induce scarring disease of the ocular mucosa, known as trachoma, the most common infectious cause of blindness worldwide. We hypothesized that epithelial-mesenchymal transition (EMT) contributes to the fibrotic process in trachomatous scarring. …”
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  17. 37
    “…Participants must meet the following inclusion criteria: a) guardians having a child age 3 years, b) participating to annual health checkup in child health clinic, c) at least one of the guardian is able to understand the languages that intervention is provided. …”
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  18. 38
    “…Written informed consent will be obtained from the parents or legal guardian and from the children. Research findings will be disseminated in peer-reviewed journals and scientific meetings. …”
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  19. 39
    “…Patients are eligible to be included in the trial if they are over 60 years of age and they, or their family or guardian, give written consent. Participants are randomised into three groups. …”
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  20. 40
    “…IMPORTANCE: Accurate diagnosis of retinopathy of prematurity (ROP) is essential to provide timely treatment and reduce the risk of blindness. However, the components of an ROP examination are subjective and qualitative. …”
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