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Clinical Trials/NCT02610608
NCT02610608TerminatedNot Applicable

Assistance Médicale à la Procréation et Risque Thrombotique

University Hospital, Brest9 sites in 1 country129 target enrollmentStarted: February 2, 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
129
Locations
9
Primary Endpoint
Evaluation of professional clinical practice for ovarian stimulation care

Study Overview

Brief Summary

This study aims at evaluating clincal practice regarding prevention of arterial and venous thrombosis following ovarian stimulation.

Secondary outcomes are : 1) to describe the incidence and risk factors of arterial and venous thrombosis in women undergoing assisted reproductive technology and 2)to identify the incidence and risk factors for ovarian hyperstimulation syndrome in these women

Detailed Description

All women undergoing an assisted reproductive tecnology in order to receive an in vitro fertilization in French centers will be included in the study. These women will be followed up until 12 months after ovarian stimulation if they get pregnant or until 3 months if the stimulation does not lead to pregnancy. Risk factors for thrombosis and ovarian hyperstimulation syndrome will be collected in each woman. At each visit, women will be asked whether arterial and/or venous thrombosis had occured.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All women undergoing ovarian stimulation in order to receive in vitro fertilization

Exclusion Criteria

  • Age<18 years
  • Women refusing to particpate in the study
  • No health coverage
  • Women under guardianship
  • Women receiving therapeutic doses of anticoagulation

Outcomes

Primary Outcomes

Evaluation of professional clinical practice for ovarian stimulation care

Time Frame: Until 12 months followin ovarian stimulation

Secondary Outcomes

  • Arterial and/or venous thrombosis(until 12 months following ovarian stimulation)
  • Risk factors for thrombosis(until 12 months following ovarian stimulation)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (9)

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