Venous Disease Clinical Trial
— ENDPCSOfficial title:
Endovascular Versus Medical Treatment for the Pelvic Congestion Syndrome
Compare the efficacy and safety of endovascular treatment with sandwich technique (controlled release coils and 2% polidocanol foam) associated with diosmin-hisperidine and ibuprofen medical treatment and only the best chronic medical treatment available diosmin-hisperidine and ibuprofen for 3 months, in women of active gynecological age carrying pelvic congestion syndrome in public assistance in Montevideo, Uruguay.
Status | Not yet recruiting |
Enrollment | 120 |
Est. completion date | October 1, 2022 |
Est. primary completion date | July 31, 2022 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Active gynecological age - Chronic pelvic pain diagnosed by gynecologist of at least 6 months of evolution. - Transvaginal duplex ultrasound: presence of periuterine varicose veins defined by veins larger than 5mm in diameter with reflux greater than 0.5 seconds on Valsava maneuvers. Exclusion Criteria: - Presence of other causes of chronic pelvic pain: endometriosis, pelvic inflammatory disease, postoperative adhesions, uterine myoma, adenomyosis, ovarian tumors, polycystic ovary. - Fibromyalgia - BMI greater than 35 - Chronic kidney disease - thrombophilia - Alterationof coagulation. - Allergy to iodinated contrast medium. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Hospital de Clínicas Dr. Manuel Quintela | Centro Cardiovascular Universitario, Centro Hospitalario Pereyra Rossell, University of the Republic, Uruguay |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Deep venous thrombosis by duplex ultrasound | Deep venous thrombosis of the iliac or femoral axis will be reported | 30 days | |
Primary | visual analogue scale (VAS) | Pain assessment 1-10 from no pain to severe | 30 days | |
Primary | visual analogue scale (VAS) | Pain assessment 1-10 from no pain to severe | 3 months | |
Primary | Lattinen index | chronic pain assessment 2-22 from low to high | 30 days | |
Primary | Lattinen index | chronic pain assessment 2-22 from low to high | 3 months | |
Primary | McGill Pain Questionnaire | subjective pain experience assessment | 30 days | |
Primary | McGill Pain Questionnaire | subjective pain experience assessment | 3 months | |
Secondary | Female sexual function index | questionnaire that assesses different domains of sexual function. 0-48 from no sexual distress to high level of sexual distress | 30 days | |
Secondary | Female sexual function index | questionnaire that assesses different domains of sexual function. . 0-48 from no sexual distress to high level of sexual distress | 3 months | |
Secondary | varicose and reflux persistance by transabdominal duplex scan | transabdominal duplex scan: varicose permeability, prescience of gonadic or iliac reflux | 30 days | |
Secondary | varicose and reflux persistance by transabdominal duplex scan | transabdominal duplex scan: varicose permeability, prescience of gonadic or iliac reflux | 3 months | |
Secondary | varicose and reflux persistance by transvaginal duplex scan | transabdominal duplex scan: varicose permeability, prescience of gonadic or iliac reflux | 3 months | |
Secondary | varicose persistance assesment by tomography | angiotomography: Varicose and conadic Patency | 3 months |
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