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The primary outcome of the study was procedure efficacy, defined as complete abortion performed on site, with no need for repeat surgical procedure in the case of D&E, or no need for any surgical intervention in the case of induction.
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The rest of the study was performed following the procedures as already described.
The study was approved by the Committee on Human Experimentation of China Medical University, and the study procedures were in accordance with ethical standards.
Specific aims of the study were to test study procedures and explore initial immune response.
The procedure of the study is presented in Figure 1.
The procedures of the study were approved by the Local Ethical Committee of Poznań University of Medical Sciences.
All participants of the study are informed about the study goals, procedures, analyses and data reporting prior to participation.
One of the major differences between the two studies was the procedure for handling patient compliance.
The study procedure was found to be feasible, but some issues were found along the way.
The study procedure was fully explained and informed consent was obtained from all the participants.
The study procedure was approved by the ethics committee of Soochow University.
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