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Clinical Trial Summary

To evaluate the endometrial and isthmic microbiota in patients with isthmocele after C-Section, and if this microbiota is similar or not with better reproductive outcomes.


Clinical Trial Description

A total of 45 subjects undergoing in vitro fertilization treatment. Fifteen patients without isthmocele will be included in the control group and 30 patients affected with isthmocele in the other group, divided in 2 subgroups: 15 with 1 previous C-Section, and 15 with 2 or more previous C-Section. Paired samples of endometrial fluid (EF) and isthmic fluid (IF) will be obtained simultaneously the day of egg retrieval. Patients will follow a protocol for all-freezing embryos or oocytes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03519763
Study type Observational
Source IVI Middle East Fertility Clinic
Contact
Status Completed
Phase
Start date June 13, 2018
Completion date February 24, 2020

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