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Medical Assistance for the Procreation and Risk of Thrombosis.

Assistance Médicale à la Procréation et Risque Thrombotique

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02610608
Acronym
AMPERT
Enrollment
129
Registered
2015-11-20
Start date
2016-02-02
Completion date
2016-11-20
Last updated
2020-07-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Embolism and Thrombosis, Ovarian Hyperstimulation Syndrome

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.

Interventions

OTHERovarian stimulation

evaluation of clincal practice regarding prevention of arterial and venous thrombosis following ovarian stimulation

Sponsors

University Hospital, Brest
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frame
Evaluation of professional clinical practice for ovarian stimulation careUntil 12 months followin ovarian stimulation

Secondary

MeasureTime frame
Arterial and/or venous thrombosisuntil 12 months following ovarian stimulation
Risk factors for thrombosisuntil 12 months following ovarian stimulation

Other

MeasureTime frame
Incidence and risk factors for ovarian hyperstimuation syndromeuntil 12 months following ovarian stimulation

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026