Quantify the Degree of Pain Relief of Pelvic Congestion Syndrome Following Gonadal Vein Embolization

Recruiting

• Conditions: Pelvic Congestive Syndrome; Pelvic Pain

• Registration Number: NCT03794466
• Lead Sponsor: University of Kansas Medical Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-1-3
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 30

Inclusion Criteria

Inclusion Criteria:<br><br> - Female patients 18 years of age or older<br><br> - Meet the clinical and imaging criteria for the diagnosis of PCS and have no<br> contraindications to coil embolization of the gonadal veins.<br><br> - Patients who are treated with coil embolization of the gonadal veins in the<br> Interventional Radiology division between October 1, 2018 to October 1, 2019.<br><br>Exclusion Criteria:<br><br> - Patients less than 18 years of age.<br><br> - Patients who are found to have an underlying cause of pelvic congestion syndrome<br> unrelated to venous congestion and insufficiency. This includes, but is not limited<br> to, nutcracker syndrome, or a mass resulting in extrinsic compression of the gonadal<br> veins.<br><br> - Patients who have received prior surgical therapy for PCS, including bilateral<br> salpingo-oophorectomy (TAH-BSO), gonadal vein resection, or gonadal vein ligation.

Exclusion Criteria

Not provided

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quantify pain relief using the Pelvic Congestion Symptom Pain Scale after gonadal vein embolization

Secondary Outcome Measures

Name	Time	Method
Predict positive or poor response to gonadal vein embolization treatment