Pelvic congestion syndrome: diagnosis and treatment.
Elizabeth A Ignacio, Ruchika Dua, Shawn Sarin...
https://pubmed.ncbi.nlm.nih.gov/21326577Actively Recruiting
Led by University of Kansas Medical Center · Updated on 2026-03-23
30
Participants Needed
1
Research Sites
52 weeks
Total Duration
Chronic pelvic pain affects nearly 40% of women during their lifetime, with pelvic congestion syndrome (PCS) responsible for up to 30% of these cases. PCS is caused by problems in the gonadal veins, leading to painful swelling in the pelvic veins. While medical treatments aim to reduce ovarian function and tighten the veins, they often provide limited and short-term relief. This research aims to measure how much pain relief patients experience after undergoing coil embolization of the gonadal veins and to identify factors that predict better or worse outcomes. Participants will have coil embolization of the gonadal veins, a procedure performed to block the veins causing the congestion. This study observes patients treated in the Interventional Radiology division between October 2018 and October 2019. The degree of pain relief will be assessed over time, focusing especially on changes from before the procedure to one year after. Women in the study will be assessed using the Pelvic Congestion Symptom Pain Scale at baseline and up to 360 days after the embolization. Researchers will monitor pain levels and analyze clinical or imaging characteristics that might predict treatment response. The total participation time covers one year post-procedure, during which pain and treatment outcomes will be carefully tracked.
CONDITIONS
Quantify the Degree of Pain Relief of Pelvic Congestion Syndrome Following Gonadal Vein Embolization
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 12 months after the procedure
Participants who have undergone gonadal vein embolization are observed to quantify pain relief over time using the Pelvic Congestion Symptom Pain Scale.
Total: 1 location
1
The University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Actively Recruiting
C
Carissa Walter, MPH
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Have more questions? Get in touch with our team for quick support
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Elizabeth A Ignacio, Ruchika Dua, Shawn Sarin...
https://pubmed.ncbi.nlm.nih.gov/21326577Marlene T O'Brien, David L Gillespie
https://pubmed.ncbi.nlm.nih.gov/26993690Sonya Koo, Chieh-Min Fan
https://pubmed.ncbi.nlm.nih.gov/24840963Anthony James Lopez
https://pubmed.ncbi.nlm.nih.gov/25804635Jane P Daniels, Rita Champaneria, Laila Shah...
https://pubmed.ncbi.nlm.nih.gov/27397619Candace L Brown, Magda Rizer, Ryan Alexander...
https://pubmed.ncbi.nlm.nih.gov/29628614Jose A Guirola, Maria Sánchez-Ballestin, Sergio Sierre...
https://pubmed.ncbi.nlm.nih.gov/29174618