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Collaborative patients, or relatives of poorly oriented subjects were adequately informed, and approved the treatment and follow-up.
The medical ethics committee of our university medical center was informed and approved the design of our study.
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Written informed consent was obtained and approved by the Swedish ethical committee.
Relatives were informed about the treatment and approved this regimen.
The Cantonal Ethics Committee of Berne was informed prior to treatment and approved therapy.
The HBB study protocol and informed consents were submitted and approved by the Institutional Review Boards of the participating clinical sites and RTI International, as the data center.
All animal owners received and approved an informed client consent form.
Study protocol and informed consent document were reviewed and approved by Hill Top's Institutional Review Board.
The final protocol, amendments, and informed consent documentation were reviewed and approved by the study center institutional review board.
The final protocol, amendments, and informed consent documentation were reviewed and approved by the study center's Institutional Review Board.
The study design, procedures and informed consent were approved by The University of Sydney Human Ethics Committee.
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