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Clinical Trials/NCT04479059
NCT04479059
Completed
Not Applicable

Endometrial Follicular Fluid Flushing and IVF Outcome

Zeynep Kamil Maternity and Pediatric Research and Training Hospital0 sites100 target enrollmentOctober 1, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Clinical Pregnancy
Sponsor
Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Enrollment
100
Primary Endpoint
Clinical pregnancy
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Objective: In this study, our aim will be investigating the pregnancy results in unexplained infertile women undergoing ICSI, by flushing the endometrial cavity with folliculer fluid, that we maintain mature follicules inside them in oocyte retrieval day.

Study Design: 100 subfertile women who applied to Zeynep Kamil Hospital, In Vitro Fertilization Center between October 2016 to May 2017 will be randomized with computer generated programme. The patients will be divided into two groups; follicular fluid group (n=50) and control group (n=50). The inclusion criterias are: age between 20-39 years, basal FSH level < 10 mIU/ml, body mass index<35 kg/m2 and E2 levels in human chorionic gonadotropin (hCG) day between 1000-4000 pg/ml. Patients meets these criteria will be included to the study programme. The exclusion criteria are determined as below: previously diagnosed endometriosis, uterine leiomyomas, hydrosalpinx, endocrinological disorders; previous history of implantation failure in IVF/ICSI cycles and severe male factor infertility.

Detailed Description

Objective: In this study, our aim will be investigating the pregnancy results in unexplained infertile women undergoing ICSI, by flushing the endometrial cavity with folliculer fluid, that we maintain mature follicules inside them in oocyte retrieval day. Study Design: 100 subfertile women who applied to Zeynep Kamil Hospital, In Vitro Fertilization Center between October 2016 to May 2017 will be randomized with computer generated programme. The patients will be divided into two groups; follicular fluid group (n=50) and control group (n=50). The inclusion criterias are: age between 20-39 years, basal FSH level \< 10 mIU/ml, body mass index\<35 kg/m2 and E2 levels in human chorionic gonadotropin (hCG) day between 1000-4000 pg/ml. Patients meets these criteria will be included to the study programme. The exclusion criteria are determined as below: previously diagnosed endometriosis, uterine leiomyomas, hydrosalpinx, endocrinological disorders; previous history of implantation failure in IVF/ICSI cycles and severe male factor infertility.

Registry
clinicaltrials.gov
Start Date
October 1, 2016
End Date
May 31, 2017
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Responsible Party
Principal Investigator
Principal Investigator

Faik Uzun

research assistant

Zeynep Kamil Maternity and Pediatric Research and Training Hospital

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • previously diagnosed endometriosis, uterine leiomyomas, hydrosalpinx, endocrinological disorders; previous history of implantation failure in IVF/ICSI cycles and severe male factor infertility.

Outcomes

Primary Outcomes

Clinical pregnancy

Time Frame: during last 24 months

intrauterine pregnancy with metal cardiac activity

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