Sentence examples for before study initiation in from inspiring English sources

Written informed consent was obtained from participants (mothers) before study initiation, in accordance with both Brigham and Women's Hospital and Beth Israel Deaconess Medical Center Human Subjects Committees.

All participating hospitals were required to obtain local institutional review board approval before study initiation in addition to institutional review board approval obtained at the study coordinating and data analysis center at Duke University.

The exclusion criteria were: fever (≥38°C) during the last 48 hours before study initiation, participation in another clinical trial during the last 3 months, use of an immunosuppressive agent, pregnancy, breastfeeding, and positive fecal occult blood test.

The study protocol and amendments were approved by institutional review boards or independent ethics committees before study initiation, and the study was conducted in accordance with the Declaration of Helsinki.

The protocol, amendments, and patient informed consent were approved by the institutional review board(IRB /independent ethics committee (IEC) at each site before study initiation, and the study was performed in accordance with the Declaration of Helsinki and the International Conference on Harmonisation/Good Clinical Practice.

We registered the study protocol in Clinical Trials before study initiation (Clinicaltrials.gov: NCT02074072).

The study protocol was approved by an independent ethics committee/institutional review board and regulatory agency in each centre (as appropriate) before study initiation.

The study team did not perform community sensitization to raise awareness of the new iCCM models that were being evaluated in the CMS catchment area before study initiation.

The study protocol (ClinicalTrials.gov ID: NCT00763971) was approved by an independent ethics committee/institutional review board and regulatory agency in each centre (as appropriate) before study initiation.

The study protocol was approved by local ethics committees before study initiation, and all patients provided written informed consent before inclusion in the trial.

Each participating PPMI site received approval from a local research ethics committee before study initiation and obtained written informed consent from all subjects participating in the study.