Carlos Roberto de Mello RiederJonas Alex Morales SauteRaphael Machado de CastilhosThais Lampert MonteArtur Schumacher SchuhKarina Carvalho DonisAline Dutra RussoGabriele Nunes SouzaMaria Luiza Saraiva-PereiraClinical Study Protocol. FIRM-ACT. Collaborative group for Adrenocortical Carcinoma Therapy. . 2004...
22,32 The protocol should acknowledge and summarize these issues, with full details provided in the statistical analysis plan. Methods: Monitoring SPIRIT-22-PRO Extension: State whether or not PRO data will be monitored during the study to inform the clinical care of individual trial participants ...
Study protocol of a phase 1 clinical trial establishing the safety of intrapleural administration of liposomal curcumin: curcumin as a palliative treatment... Introduction This is a phase 1, open-label, single-centre, uncontrolled, dose-escalation study to evaluate the feasibility, tolerability and ...
Complicated Odontogenic Infections at 2 District Hospitals in Tonkolili District, Sierra Leone: Protocol for a Prospective Observational Cohort Study (DELAY). JMIR Res. Protocol. 2021, 10, e33677. [Google Scholar] [CrossRef] [PubMed] Disclaimer/Publisher’s Note: The statements, opinions and data...
Informed consentaddresses the first concern, while providing the appropriate safeguards concerning adverse events requires specification in the research protocol of the conditions, thresholds, and consequences of breaking the code (unblinding the study). A related problem with ethical implications is the...
# - Get trial data result <- dbGetFieldsIntoDf( fields = c( "ctrname", "record_last_import", # CTGOV2 "protocolSection.statusModule.startDateStruct.date", "protocolSection.statusModule.overallStatus", # EUCTR "n_date_of_competent_authority_decision", "trialInformation.recruitmentStartDate"...
2.1. Study Protocol The systematic review and its methods were approved and registered on the International Prospective Register of Systematic Reviews (PROSPERO) under the protocol number CRD42021247588. This study was conducted and reported in accordance with the Preferred Reporting Items for Systematic ...
Every clinical trial follows a protocol that describes what types of people may participate in the trial; outlines the exact schedule of tests, procedures, medications, and/or dosages involved in the trial; and specifies the length of the study. Each trial has specific inclusion and exclusion cr...
Utilize workflows to manage CDA, protocol amendments, site identification surveys, and prestudy visits Enable data-driven business decisions and transparency for regulatory compliance and risk mitigation Driving Site Activation Accelerating site activation can jumpstart a clinical trial, but with the hours ...
Preterm-birth-prevention withLactobacillus crispatusoral probiotics: Protocol for a double blinded randomised placebo-controlled trial (the PrePOP study) Gillian A. Corbett, ... Fionnuala M. McAuliffe February 2025View PDF Research articleAbstract only ...