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NCT03794466

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

Recruiting now Last updated 23 March 2026
What this trial tests

trial in Pelvic Congestive Syndrome in 30 participants. Currently enrolling.

Timeline
10 May 2019
Primary endpoint
31 December 2026
31 December 2027

Quick facts

Lead sponsorUniversity of Kansas Medical Center
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment30
Start date10 May 2019
Primary completion31 December 2026
Estimated completion31 December 2027
Sites1 location across United States

Conditions studied

Sponsor

University of Kansas Medical Center

Who can join

18 and older, female only, with Pelvic Congestive Syndrome or Pelvic Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Pelvic Congestive Syndrome

Currently open trials in the same condition.

Other University of Kansas Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03794466.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing