Myoma Microvascularization Analysis Using Sonovue Before and After Uterine Artery Embolization

Sponsor
University Hospital, Tours (Other)
Overall Status
Unknown status
CT.gov ID
NCT00351494
Collaborator
(none)
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Study Details

Study Description

Brief Summary

Contrast-enhanced ultrasound is supposed to improve the detection of myomas as well as improve the follow-up after specific treatments like embolization. It will also help the investigators better understand the mechanism of success or failure for embolization and could reduce the amount of particles injected by determining the endpoint of the procedure in order to treat the myomas while preserving the myometrium.

Condition or Disease Intervention/Treatment Phase
  • Procedure: contrast enhanced ultrasonography
  • Procedure: embolization

Detailed Description

Before embolization of the uterine artery, 40 patients with unique or multiple myomas will be included prospectively in our study and evaluated with sonography before and after injection of Sonovue (2.4 ml) (Bracco Int Milano Italy). Pelvic ultrasound with contrast enhancement will be done the day after and six months after the procedure.

Microvascularization of the myomas and the endometrium will be described. Some tiny myomas which are not visible on conventional sonography could be identified for a perfect matching with MRI detection.

Study Design

Study Type:
Observational
Anticipated Enrollment :
40 participants
Time Perspective:
Prospective
Official Title:
Myoma Microvascularization Analysis Using Sonovue Before and After Uterine Artery Embolization
Study Start Date :
Jul 1, 2006
Anticipated Study Completion Date :
Jun 1, 2009

Outcome Measures

Primary Outcome Measures

  1. To investigate the usefulness of contrast-enhanced ultrasound with real-time imaging technique in the assessment of vascular patterns from myomas myometrium and ovaries before and after uterine artery embolization [Inclusion period and follow-up]

Secondary Outcome Measures

  1. Accordance between contrast-enhanced imaging and IRM [inclusion period and follow-up]

  2. Accordance between early vascular patterns due to embolization of the fibroma and the success of the technique which is evaluated after 6 month [inclusion period and follow-up]

  3. Relationship between the post embolization pain and the vascular change of the fibroma and the myometrium [inclusion period]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Uterine myomas with solid tissue (greater diameter lower than 15 cm)

  • The embolization is planified during the 15 days after the contrast ultrasonography

  • Written informed consent is signed

Exclusion Criteria:
  • Intracavitary uterine mass possibly due to a polyp or endometrial cancer

  • Necessity of using the endovaginal way of ultrasonography because of the myoma's size and accessibility

  • Menopause

  • Pregnancy and breastfeeding

  • Recent cardiac affection

  • History of acute cardiac disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre d'Innovation Technologique-Ultrasons Tours France 37344

Sponsors and Collaborators

  • University Hospital, Tours

Investigators

  • Principal Investigator: Henri MARRET, Pr, Service de Gynécologie Obstétrique CHRU TOURS
  • Study Director: François TRANQUART, Pr, Centre d'Innovation Technologique CHRU TOURS

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00351494
Other Study ID Numbers:
  • HP06-HM/FIBROME
First Posted:
Jul 13, 2006
Last Update Posted:
Nov 22, 2007
Last Verified:
Nov 1, 2007
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 22, 2007