Mostrando 61 - 80 Resultados de 84 Para Buscar 'Blind Guardian', tiempo de consulta: 0.49s Limitar resultados
  1. 61
    “…Informed consent will be obtained from all participants or their guardians. Upon completion, the authors will submit their findings to a peer-reviewed journal or academic conference for publication. …”
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    Effects of high-intensity interval training, moderate-intensity continuous training, and guideline-based physical activity on cardiovascular metabolic markers, cognitive and motor function in elderly sedentary patients with type 2 diabetes (HIIT-DM): a protocol for a randomized controlled trial
  2. 62
    “…All the monocular blind children of this study were from the urban area. …”
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    Eye Injuries Among Primary School Children in Enugu, Nigeria: Rural vs Urban
  3. 63
    “…After excluding patients receiving a relaparotomy via another site, a questionnaire about the appearance of the umbilicus was completed by the patients’ guardians at postoperative month 6 to assess satisfaction and determine the visual analog scale score. …”
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    Vertical Umbilical Incision Achieves Better Cosmesis Than Periumbilical Incision in Neonates and Infants
  4. 64
    “…BACKGROUND: The majority of childhood blindness causes in low-income countries are treatable or avoidable. …”
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    Exploring the knowledge, attitudes, and practice towards child eye health: A qualitative analysis of parent experience focus groups
  5. 65
    “…With the aim of determining if application of a ceramide-dominant emollient two times per day reduces the risk of AD and food allergy, we have commenced a multicentre phase III, outcome assessor blinded, randomised controlled trial of this emollient applied from birth to 6 months. …”
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    PEBBLES study protocol: a randomised controlled trial to prevent atopic dermatitis, food allergy and sensitisation in infants with a family history of allergic disease using a skin barrier improvement strategy
  6. 66
    “…Each class was allocated to the intervention group (IG, n = 21) or the waiting list control group (WLCG, n = 17) with single-blinded randomization. MHL was assessed using the QuALiSMental. …”
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    Adolescents’ Empowerment for Mental Health Literacy in School: A Pilot Study on ProLiSMental Psychoeducational Intervention
  7. 67
    “…No licensed Shigella vaccine is presently available globally. A double-blinded, randomized, placebo-controlled, age descending phase II clinical trial of a bivalent conjugate vaccine was studied in China. …”
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    Safety and Immunogenicity of a Shigella Bivalent Conjugate Vaccine (ZF0901) in 3-Month- to 5-Year-Old Children in China
  8. 68
    “…The blinded primary outcomes at 7 months of age are immunogenicity of specific vaccine antigens (geometric mean concentration (GMC) and proportion of participants with above threshold GMC of 0.35 µg/L). …”
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    Pneumococcal conjugate vaccines PREVenar13 and SynflorIX in sequence or alone in high-risk Indigenous infants (PREV-IX_COMBO): protocol of a randomised controlled trial
  9. 69
    “…METHODS: This is a patient- and assessor-blinded randomized controlled clinical trial. Participants (n = 110) will receive S-ketamine (0.5 mg/kg) or midazolam (0.08 mg/kg) intravenously administrated at a ratio of 1:1 in the anaesthesia holding area. …”
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    Comparison of S-ketamine and midazolam for intravenous preoperative sedative and anxiolytic effects in preschool children: study protocol for a randomized controlled clinical trial
  10. 70
    “…Earlier detection of ROP-related proliferation may prevent vitreoretinal traction, retinal detachment, and blindness.…”
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    Peripheral OCT Assisted by Scleral Depression in Retinopathy of Prematurity
  11. 71
    “…METHODS AND ANALYSIS: This non-blinded, multicentre, randomised controlled trial will recruit 198 preterm born infants with moderate or severe BPD between 36 and 38 weeks PMA. …”
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    Supplemental oxygen strategies in infants with bronchopulmonary dysplasia after the neonatal intensive care unit period: study protocol for a randomised controlled trial (SOS BPD study)
  12. 72
    “…Outcome assessors will be blinded of study design and group allocation. The primary outcome is the mean difference in days between discharge and entry. …”
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    Effectiveness of osteopathic manipulative treatment in neonatal intensive care units: protocol for a multicentre randomised clinical trial
  13. 73
    “…Consent for publication will be obtained from all parents or legal guardians. Results of this study will be reported in full through peer-reviewed journals. …”
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    Pulp liner materials in selective caries removal: study protocol for a randomised controlled trial
  14. 74
    “…Patients will receive either pre-emptive administration of a bolus dose of 60–70 mg/kg fibrinogen concentrate (Riastap®) or placebo 0.9 % saline in equal volume to active treatment, both given as intravenous infusion blinded for the person administering the infusion. …”
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    Pilot Randomized trial of Fibrinogen in Trauma Haemorrhage (PRooF-iTH): study protocol for a randomized controlled trial
  15. 75
    por Kocaturk, Ozlem, Keles, Sultan
    Publicado 2018
    “…The recovery time, satisfaction levels of parents or guardians, extubation time, duration of the operation, and type of dental procedure were also recorded. …”
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    Recovery characteristics of total intravenous anesthesia with propofol versus sevoflurane anesthesia: a prospective randomized clinical trial
  16. 76
    “…Investigators not involved in the running of the trial, outcome assessors, and the statistician will be blinded to the group allocation until the analysis is completed. …”
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    Hand sanitisers for reducing illness absences in primary school children in New Zealand: a cluster randomised controlled trial study protocol
  17. 77
    “…Data capture forms and questionnaires were used to record the children’s medical and dental history based on clinical chart review and recall from their parents/guardians. Dental examinations were performed by calibrated dentists blinded to the study grouping. …”
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    Prevalence and associated factors of enamel developmental defects among Nigerian children with perinatal HIV exposure
  18. 78
    “…Informed consent will be obtained from guardians of all participants in addition to assent from participants. …”
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    Adaptive randomised controlled non-inferiority multicentre trial (the Ketodex Trial) on intranasal dexmedetomidine plus ketamine for procedural sedation in children: study protocol
  19. 79
    “…It generates referrals, automated short messages service (SMS) notifications to patients or guardians and has a program dashboard for visualising service delivery. …”
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    Peek Community Eye Health - mHealth system to increase access and efficiency of eye health services in Trans Nzoia County, Kenya: study protocol for a cluster randomised controlled trial
  20. 80
    “…Parents or guardians must provide written informed consent. Eligible participants are 2–11 years with evidence of P. falciparum malaria infection by peripheral blood smear or rapid diagnostic test with CNS symptoms associated with malaria. …”
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    Aggressive antipyretics in central nervous system malaria: Study protocol of a randomized-controlled trial assessing antipyretic efficacy and parasite clearance effects (Malaria FEVER study)
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