Mostrando 47,461 - 47,480 Resultados de 47,543 Para Buscar '"ethics"', tiempo de consulta: 0.68s Limitar resultados
  1. 47461
    “…Associated risk factors and the strengths of association are summarized using odds ratios (ORs) and 95% confidence intervals. Ethical clearance was obtained from MUHAS Senate Research and Publications Committeeand permission sought from the administration of KCMC. …”
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  2. 47462
    “…However, embryo selection raises ethical concerns. Thus, several techniques to select sex-specific spermatozoa have been proposed but carry limitations. …”
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  3. 47463
    “…WIDER IMPLICATIONS OF THE FINDINGS: Consuming less resources without negatively impacting on health outcomes carries ethical and practical implications for individuals and the community, as this approach may result in overall increased healthcare access. …”
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  4. 47464
    “…All data on biomarkers will be presented graphically over time. RESULTS: No ethical approval will be required, as this review is based on published data and does not involve interaction with human participants. …”
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  5. 47465
    “…Methods: All research and data-sharing were conducted with participant/guardian consent and institutional ethical approval. We defined CDP as puberty starting between 12 and 18 y in girls and between 13.5 and 18 y in boys and IHH as low sex steroids and non-elevated gonadotropins at ≥18 y, both with no cause identified on standard clinical evaluation. …”
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  6. 47466
  7. 47467
    “…LIMITATIONS, REASONS FOR CAUTION: The numbers of participants both in the prevalence study and in pregnancy did not reach the a priori estimated numbers. For ethical reasons, the patients with preconception TSH >4.5 mIU/l were treated with thyroxine. …”
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  8. 47468
    “…All participants continued with their usual care for ethical reasons. The SA group’s treatment protocol consisted of 6 acupuncture points on the auricular pavilion chosen according to the diagnosis of depression by traditional Chinese medicine (Shenmen, subcortex, heart, lung, liver, and kidney). …”
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  9. 47469
    “…Search terms used across all six electronic databases were: (‘advanced parental age’ OR ‘advanced maternal age’ OR ‘advanced paternal age’ OR ‘advanced reproductive age’ OR ‘late parent*’ OR ‘late motherhood’ OR ‘late fatherhood’) AND (‘IVF’ OR ‘in vitro fertilization’ OR ‘in-vitro-fertilization’ OR ‘fertilization in vitro’ OR ‘ICSI’ OR ‘intracytoplasmic sperm injection’ OR ‘reproductive techn*’ OR ‘assisted reproductive technolog*’ OR ‘assisted reproduction’ OR ‘assisted conception’ OR ‘reproduction’ OR ‘conception’ OR ‘birth*’ OR ‘pregnan*’) AND (‘wellbeing’ OR ‘well-being’ OR ‘psycho-social’ OR ‘social’ OR ‘ethical’ OR ‘right to reproduce’ OR ‘justice’ OR ‘family functioning’ OR ‘parental competenc*’ OR ‘ageism’ OR ‘reproductive autonomy’ OR ‘outcome’ OR ‘risk*’ OR ‘benefit*’). …”
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  10. 47470
    “…Randomized clinical trials of the efficacy of early intervention for children with CHL hearing losses are inappropriate because of ethical reasons. Prospective cohort studies with long-term outcomes of rare diseases are costly, take a long time and simultaneously substantial benefits of early intervention for language development seem likely. …”
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  11. 47471
    “…These websites violate professional, legal, and ethical standards and endanger patient safety. This work shows evidence that online pharmacies that act illegally appear to have greater longevity than others, presumably because there is no compelling reason for frequent change in order to survive. …”
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  12. 47472
    “…All participants of the study signed written consent approved by the pilot institution’s Ethical Committee. Demographic information, including age, ethnic origin, and primary language, was obtained from the respondents. …”
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  13. 47473
    “…Endometrial biopsies were collected with institutional ethical approval and written informed consent. Concentrations of mRNAs encoded by steroid receptors, P-regulated genes and factors in decidualised endometrium were quantified with qRT-PCR. …”
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  14. 47474
    “…The main limitations of this study include the lack of a control group, which was not included due to ethical considerations; clinical study requirements imposed when PrEP was not approved through the regulatory system, which could have affected uptake; and the timing of the implementation of a national sex worker HIV programme, which could have also affected uptake and retention. …”
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  15. 47475
    “…METHODS: Seventy-one consenting adult (M=33, F=38; mean age 30.87 ± 9.59 years, mean duration of illness 89.68 ± 77.98 months) patients, with a diagnosis of Schizophrenia, were randomly assigned to receive bilateral ECT with either 0.5ms (n=35) or 1.5ms (n=36) PW stimulus; after obtaining institutional ethical-committee’s approval. Seizure threshold was determined during the first session. …”
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  16. 47476
    “…The study was approved by the local Ethical Review Boards. All participants underwent a comprehensive socio-demographic and clinical evaluation at baseline and after 6, 12 and 18 months follow-up to identify which individuals converted to psychosis (UHR-P) and which did not (UHR-NP). …”
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  17. 47477
    “…METHODS: Using G*Power 3.1 software with effect size f (0.8), total sample size was calculated from data obtained from a previous study on working memory performance in NMDAR encephalitis for the 3 groups (NMDAR encephalitis, healthy controls & schizophrenia) (N=30). Following ethical approval, 12 individuals diagnosed with NMDAR encephalitis were recruited from neurological centres. …”
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  18. 47478
    “…Those seeking to coproduce interventions or utilise RCT designs should consider tensions between data quality and intervention implementation and ethical issues regarding control groups. Conclusion This paper confirms previous research confirming the benefits of coproduction. …”
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  19. 47479
    “…The National Regional Ethical Committee (REC) 2014/ 684/ REK-Nord. https://helseforskning.etikkom.no/prosjekterirek/prosjektregister/prosjekt?…”
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  20. 47480
    “…Adaptive enrichment designs and strategies are important components of a rational approach to achieve clinical research objectives in shorter clinical trial timelines and with increased cost-effectiveness without compromising ethical standards or the overall statistical integrity of the study. …”
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