Pelvic Pain Clinical Trial
Official title:
Assessment of Pain of Pelvic Congestion Syndrome Treated by Coils Embolization (SCVPC)
Summary:
Main Objective: to evaluate the efficacy of pelvic gonadal vein embolization with coils in
treatment of pelvic congestion syndrome Methods: retrospective study included 25 patients in
the University hospital of Brest.
The Primary Outcome Measure: To evaluate (to measure) pain relief using visual analogous
scale (VAS) before and after gonadal vein embolization for pelvic congestion syndrome The
Secondary Outcome Measures were to assess the impact of the treatment on specific and general
symptoms through a survey.
A retrospective, non-invasive monocentric study of our Hospital 10-year registry (including
data on MRI angiography and Vascular Doppler Ultrasound) of patients who have already
undergone coil embolization of pelvic gonadal vein in treatment of pelvic congestion
syndrome. These patients will be contacted by phone to participate in the study. An
information letter will be handed out and the study protocol will be explained to the
patients. After obtaining their written consent, they will be asked to fill out the study's
validated questionnaire at home and return it to us through pre-paid regular mail. A face to
face interview with the patient will be scheduled to assess the correlation between patient's
clinical symptoms and survey results. There will be no change in patient's routine follow-up
care.
All physician investigators of the study are experts in their field of medicine (e.g.
interventional MRI angiography, vascular disease).
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