The human subject protocol involved in this study has been approved by University of California, Irvine (UCI) and Kenya Medical Research Institute (KEMRI).
The mice and the protocol involved in the study had been approved by Institutional Animal Care and Use Committee (IACUC).
As an insider, he was co-chairman of the National Committee for Protocol Finalisation and as an outsider, he was involved in this study as a researcher.
This study was approved by the Ethics Committee of Yokohama City University Graduate School of Medicine, and written informed consent was obtained from all patients involved in this study (notice of approval Institutional Review Board protocol number: B1100513031).
This set of EMDR protocols was developed by the principal investigator and the EMDR International Association (EMDRIA -approved consultant involvEMDRIA -approved as a trainer.
Informed consent to the protocol approved by the Ethical Committee of Hospital Clínico San Carlos (Madrid, Spain) was obtained from the women involved in this study.
All subjects involved in this study provided written informed consent under a protocol adherent to the Helsinki Guidelines and approved by the Institutional Review Board of the Helsinki University Central Hospital.
All patients were treated according to the same treatment protocol for PPH, summarised in the decision algorithm approved by the three departments involved in this study (Figure 1).
All necessary consents from all patients involved in this study were obtained according to each aforementioned IRB protocol.
All necessary consents from all patients involved in this study were obtained according to the aforementioned ethics protocol.
