Glue Embolization vs Conservative Treatment for Pelvic Congestion Syndrome
Condition(s) studied
Investigational drug(s) / intervention(s)
Micronized purified flavonoid fraction (Daflon ®): Patients will receive micronized purified flavonoid fraction (Daflon ®), 500 mg twice/daily for 3 months.
Glue embolization: Patients will receive transcatheter glue embolization.
Study summary
The aim of this study is to compare glue embolization and conservative treatment for pelvic congestion syndrome regarding safety and efficacy.
Eligibility
Primary outcome measure(s)
- Degree of pain — Post intervention for 3 months
Degree of pain will be assessed using a Visual Analog Scale (VAS). The VAS is a self-reported scale consisting of a horizontal or vertical line, usually 10 cm long. An introductory question asks the patient to mark a point on the line that best refers to his or her pain. Patients will be encouraged to assess the intensity of subjective manifestation of each symptom by scoring from 0 (no symptom) to 10 (the most extreme manifestation possible).
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Tanta University | Tanta | ElGharbia | Recruiting |
More Tanta University trials in Egypt
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06560294 on ClinicalTrials.gov ↗ ← All trials in Egypt