Actively Recruiting
Quantify the Degree of Pain Relief of Pelvic Congestion Syndrome Following Gonadal Vein Embolization
Led by University of Kansas Medical Center · Updated on 2026-03-23
30
Participants Needed
1
Research Sites
451 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The primary objective is to quantify the degree of pain relief in patients undergoing gonadal vein embolization with coils as well as identify clinical or imaging factors that are predictive of a positive response to treatment, or poor response to treatment.
CONDITIONS
Official Title
Quantify the Degree of Pain Relief of Pelvic Congestion Syndrome Following Gonadal Vein Embolization
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female patients 18 years of age or older
- Meet the clinical and imaging criteria for the diagnosis of PCS and have no contraindications to coil embolization of the gonadal veins
- Patients who are treated with coil embolization of the gonadal veins in the Interventional Radiology division between October 1, 2018 to October 1, 2019
You will not qualify if you...
- Patients less than 18 years of age
- Patients with an underlying cause of pelvic congestion syndrome unrelated to venous congestion and insufficiency, including nutcracker syndrome or a mass causing compression of the gonadal veins
- Patients who have received prior surgical therapy for PCS, including bilateral salpingo-oophorectomy, gonadal vein resection, or gonadal vein ligation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Actively Recruiting
Research Team
C
Carissa Walter, MPH
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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