To identify specific clinical trials, the researcher can restrict the search in the identifiers section with a clinical trial registry number from ClinicalTrials.gov (NCT ID) or a secondary source ID. In the section participant details, the fields “gender”, “minimum age of the participant”...
This participant was not included in the largest full analysis set (ie, modified intention-to-treat analysis). Participants could remain in the study after discontinuing trial medication and complete the trial assessments until week 24 for completion of the study. The full analysis set for the ...
The multisite randomized controlled trial consisted of adult men and women (n=507) entering 10 outpatient addiction treatment programs who were randomly assigned to receive 12 weeks of either treatment as usual (n=252) or treatment as usual plus TES, with the intervention replacing about 2 hours...
Randomized, placebo-controlled, participant- and assessor-blinded trial involving 102 community volunteers with hip pain levels of 40 or higher on a VAS of 100 mm (range of 0 to 100 mm; 100 indicates worst pain possible) and hip OA confirmed by radiograph were included for analysis. A tota...
Important considerations include study aims, timing, breadth and depth of the existing infrastructure that can be leveraged, participant burden, likely participation rate and available sample size in the cohort, required sample size for the trial, and investigator expertise. Community engagement and ...
74.Participant Preferences for the Provision of Registration Trials Results 机译:提供注册试用结果的参与者首选项 作者:Soichiro Tajima;Akiyo Akaishi;Toshiko Miyamoto;Rumi Katashima;Kenichi Nakai;Takao Mitsui;Hiroaki Yanagawa 期刊名称:《Journal of Clinical Medicine Research》 | 2013年第5期 关键词: Re...
The design of this trial has been published,15 and the trial protocol is available in Supplement 1. Written informed consent was collected, and the study was approved by the Chonnam National University Hospital (CNUH) Institutional Review Board. Participant recruitment and study flow are presented...
If a participant needs emergency treatment, blinding will be broken, and the participant will then be managed as off-trial. Blinding The participants, nurses, neuroimaging specialists, statisticians, and psychologists are all blind to group allocation. Data management, evaluation, and analysis will...
They also included trials where both eyes from 1 participant received different treatments. These investigators used standard methodological procedures recommended by Cochrane; 2 authors independently reviewed all the titles and abstracts identified from the electronic and manual searches against the ...
Each trial has eligibility criteria (in unstructured natural language) that describe criteria for enrolling patients, including participant characteristics such as age, gender, medical history, target disease conditions, and current health status. Definition 3 (trial eligibility criteria) The patient group...