Evaluation of the Sanitary Safety of a Healthcare Professional Conference Held 9-11 June 2021 at the Paris Congress Centre
Condition: Covid19 Intervention: Other: Exposure to the FICS annual meeting (June 9-11 2021, Paris Congress Center) Sponsor: French Society for Intensive Care Not yet recruiting (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - June 8, 2021 Category: Research Source Type: clinical trials
Protocol for the development of a core outcome set for lateral elbow tendinopathy (COS-LET)
ConclusionsThere is currently no COS for the measurement or monitoring of LET in trials or clinical practice. The output from this project will be a minimum COS recommended for use in all future English language studies related to LET. The findings will be published in a high-quality journal and disseminated widely using professional networks, social media and via presentation at international conferences.Trial registrationRegistered with the Core Outcome Measures in Effectiveness Trials (COMET) database, November 2019.https://www.comet-initiative.org/Studies/Details/1497. (Source: Trials)
Source: Trials - May 10, 2021 Category: Research Source Type: clinical trials
Effectiveness of TechCR Among CHD Patients
Condition: Coronary Heart Disease Interventions: Behavioral: exercise training for TechCR; Behavioral: audio/video conference; Behavioral: educational video; Behavioral: Daily log; Behavioral: exercise training for centre-based Sponsor: Chinese University of Hong Kong Recruiting (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - April 28, 2021 Category: Research Source Type: clinical trials
Prophylactic use of dural tenting sutures in elective craniotomies in adults —is it necessary? A study protocol for a multicentre, investigator- and participant-blinded randomised, parallel-group, non-inferiority trial
This study is designed as a randomised, multicentre, double-blinded, controlled interventional trial with 1:1 allocation. About one half of the participants will undergo craniotomy without dural tenting sutures and will be considered an intervention group. The other half will undergo craniotomy with these sutures. Both groups will be followed clinically and radiologically. The primary outcome is reoperation due to extradural haematoma. Secondary outcomes aim to evaluate the impact of dural tenting sutures on mortality, readmission risk, postoperative headaches, size of extradural collection, cerebrospinal fluid leak risk a...
Source: Trials - April 12, 2021 Category: Research Source Type: clinical trials
