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Clinical Trials/NCT03317548
NCT03317548
Unknown
Not Applicable

Chung Shan Medical University Hospital

Chung Shan Medical University1 site in 1 country500 target enrollmentMay 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infertility, Female
Sponsor
Chung Shan Medical University
Enrollment
500
Locations
1
Primary Endpoint
pregnancy rate
Last Updated
8 years ago

Overview

Brief Summary

The aim of this study was to compare the clinical outcomes between fresh embryo and frozen embryo transfer in in vitro fertilization (IVF). All frozen embryo was vitrified at pronuclear stage (2PN) and cultured to cleavage embryos for transfer.

This is a retrospective study. All IVF cycles were included in this study and further divided into fresh and frozen embryo transfer groups. The collection data including: stimulation protocols, medicines, blood test results, pregnancy test and all clinical data. The primary outcome is pregnancy rate and secondary outcome is implantation rate.

Detailed Description

Study design Study progress: Stage 1: collection of all data from frozen embryo transfer and fresh embryo transfer groups. Stage 2: selection data and check the delivery outcomes Stage 3: analysis data and presentation. Including criteria: all patients who underwent IVF. Excluding criteria: No. Statistics analysis: chi-test, t-test Assessment point: Primary endpoint: pregnancy rate Secondary endpoint: implantation rate Withdraw criteria: not application. Treatments: not application. Collection number: 500 patients. Scheduled trial period: 2017.05.01\~2018.04.30 Expected research results: The implantation rate in frozen embryo transfer group which vitrified at 2PN stage is higher than fresh embryo transfer. The pregnancy rate in frozen embryo transfer group which vitrified at 2PN stage is higher than fresh embryo transfer. This study is only data analysis, no additional collection of samples. This study does not involve vulnerable groups.

Registry
clinicaltrials.gov
Start Date
May 1, 2017
End Date
April 30, 2018
Last Updated
8 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yeh

Director of The Institutional Review Board

Chung Shan Medical University

Eligibility Criteria

Inclusion Criteria

  • all patients with in vitro fertilization protocols

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

pregnancy rate

Time Frame: HCG test at day 15 after embryo transfer or day 18 after oocyte pick up

HCG test

Study Sites (1)

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