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Fertility After Diagnosis and Management of Acquired Uterine Arteriovenous Malformation

Fertility After Diagnosis and Management of Acquired Uterine Arteriovenous Malformation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03656211
Acronym
MAVUFERT
Enrollment
15
Registered
2018-09-04
Start date
2017-10-02
Completion date
2017-10-10
Last updated
2018-09-04

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

Conditions

Arteriovenous Malformations

Keywords

Uterine AVM

Brief summary

Uterine arteriovenous malformations (UAVM) are short circuits between systemic arterial and venous networks within the uterus. They are congenital or acquired (in the course of an endo-uterine gesture such as curettage or interventions such as caesareans or myomectomies). They can be manifested by severe metrorrhagia that can go as far as to put the patient's vital prognosis at risk. There are no recommendations for the management of UAVM since this pathology is rare and therefore series are performed with few cases. If some of these UAVM disappear spontaneously after a therapeutic abstention, when the clinical context allows it, in case of symptomatic UAVM, a selective embolization with arteriography is often carried out to postpone the hysterectomy of hemostasis. There are also more marginal management options such as Gonadotropin-Releasing Hormone agonists, methotrexate or curettage that are decided on a case by case basis depending on the symptoms and protocols of each medical team. Regarding subsequent fertility and pregnancy outcomes after conservative treatment, the number of studies is even lower.

Interventions

OTHERTelephone interview

Patients are contacted by telephone to know the history of the disease since the diagnosis of UAVM and the impact of management on fertility. All medical data related to the care and necessary for the study are collected from the medical file the participation of the patients is limited to a telephone interview.

Sponsors

Rennes University Hospital
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

* Major patient * Diagnosis of UAVM, symptomatic or not, between January 1st, 2000 and March 30th, 2017 confirmed by imagery performed at the Rennes University Hospital * Not against her participation in research

Exclusion criteria

* Minor patient at the time of diagnosis * congenital UAVM * Uterine malformation * Patient under legal protection (guardianship, curatorship, safeguard of justice).

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of fertilityAt the time of inclusionThe telephone interview seeks to assess fertility for all patients diagnosed with symptomatic or non-symptomatic UAVM regardless of initial management.

Secondary

MeasureTime frameDescription
Pregnancy outcomes after UAVMAt the time of inclusionThe telephone interview allows to evaluate pregnancy outcomes after diagnosis of UAVM regardless of initial management, in terms of live birth (full term or preterm birth), stillbirth, spontaneous abortion, and induced abortion.
Term of delivery after UAVMAt the time of inclusionThe telephone interview allows to evaluate the term of delivery after diagnosis of UAVM regardless of initial management
Side effects of treatments for UAVMAt the time of inclusionThe telephone interview allows to inventory the side effects of treatments
Complications of treatments for UAVMAt the time of inclusionThe telephone interview allows to evaluate the complications of treatments

Countries

France

Outcome results

None listed

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