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Establishment of Special Disease Cohort for RPLand Study of Impact Mechanism of Early Embryo Development

Sponsored by Women's Hospital School Of Medicine Zhejiang University

About this trial

Last updated 3 years ago

Study ID

IRB-20210298-R

Status

Recruiting

Type

Observational

Placebo

No

Accepting

18-75 Years
18 to 50 Years
Female
Female

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 7 months ago

What is this trial about?

Recurrent pregnancy loss (RPL) is a refractory disease with diverse etiologies, complex pathogenesis and limited therapeutic options. Current tests and treatments lack uniform specifications. This study is a prospective clinical cohort study which intends to screen out meaningful examination items and reliable and effective treatment. The study content includes (1) tracking the re-pregnancy information of patients with initial inevitable abortion, comparing the clinical data and examination test results between patients with single abortion and RPL, and (2) comprehensively and systematically screening the patients with initial inevitable abortion, taking those without obvious abnormalities and those with a re-pregnancy into the control group and taking those with a re-pregnancy after abnormal findings were treated into the study group, recording the pregnancy and perinatal conditions of the two groups, comparing the pregnancy outcomes of the two groups, and analyzing the risk factors for RPL. The results of this study will establish a model of maternal and newborn risk assessment for first trimester medication use and provide strong evidence-based evidence to clarify the diagnosis and treatment processes of RPL.

What are the participation requirements?

Yes

Inclusion Criteria

- (1) patients who were treated in the outpatient department of Zhejiang University Women's Hospital from January 1, 2018 to December 31, 2020;

- (2) With history of once spontaneous abortion;

- (3) Having fertility requirements but not yet pregnant;

- (4) Those who are willing to give birth again during the study period.

No

Exclusion Criteria

- (1) Previous history of multiple spontaneous abortion, inevitable abortion or missed abortion;

- (2) Re pregnancy after abortion, now in pregnancy or delivered;

- (3) Patients who are participating in other clinical studies or those who refuse to participate in the study;

- (4) The researchers consider that she is not suitable to participate in this study for other reasons.

Locations

Location

Status

Recruiting