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NCT02610608: AMPERT

Medical Assistance for the Procreation and Risk of Thrombosis.

Terminated Last updated 10 July 2020
What this trial tests

trial testing ovarian stimulation in Ovarian Hyperstimulation Syndrome in 129 participants. Terminated before completion.

Timeline
2 February 2016
Primary endpoint
20 November 2016
20 November 2016

Quick facts

Lead sponsorUniversity Hospital, Brest
StatusTerminated
Study typeOBSERVATIONAL
Enrollment129
Start date2 February 2016
Primary completion20 November 2016
Estimated completion20 November 2016
Sites9 locations across France

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Brest

Who can join

18 and older, female only, with Ovarian Hyperstimulation Syndrome or Cardiovascular Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other University Hospital, Brest trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02610608.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing