search
Back to results

Endovascular Versus Medical Treatment for the Pelvic Congestion Syndrome (ENDPCS)

Primary Purpose

Pelvic Congestive Syndrome, Pelvic Varices, Venous Disease

Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Medtronic® Concerto® detachable coil system
sclerosis
Diosmin / Hesperidin
Ibuprofen 400 mg
Sponsored by
Hospital de Clínicas Dr. Manuel Quintela
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pelvic Congestive Syndrome focused on measuring pelvic congestion syndrome, sclerosis, coil embolization

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

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.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Interventional treatment plus best chronic medical treatment

    Best chronic medical treatment alone

    Arm Description

    Sandwich embolization ( 2% polidocanol + Coils) Diosmin hisperidin 1g twice a day for 6 months Ibuprofen 500mg 3 times a day for 6 months

    Diosmin hisperidin 1g twice a day for 6 months Ibuprofen 500mg 3 times a day for 6 months

    Outcomes

    Primary Outcome Measures

    visual analogue scale (VAS)
    Pain assessment 1-10 from no pain to severe
    visual analogue scale (VAS)
    Pain assessment 1-10 from no pain to severe
    Lattinen index
    chronic pain assessment 2-22 from low to high
    Lattinen index
    chronic pain assessment 2-22 from low to high
    McGill Pain Questionnaire
    subjective pain experience assessment
    McGill Pain Questionnaire
    subjective pain experience assessment

    Secondary Outcome Measures

    Female sexual function index
    questionnaire that assesses different domains of sexual function. 0-48 from no sexual distress to high level of sexual distress
    Female sexual function index
    questionnaire that assesses different domains of sexual function. . 0-48 from no sexual distress to high level of sexual distress
    varicose and reflux persistance by transabdominal duplex scan
    transabdominal duplex scan: varicose permeability, prescience of gonadic or iliac reflux
    varicose and reflux persistance by transabdominal duplex scan
    transabdominal duplex scan: varicose permeability, prescience of gonadic or iliac reflux
    varicose and reflux persistance by transvaginal duplex scan
    transabdominal duplex scan: varicose permeability, prescience of gonadic or iliac reflux
    varicose persistance assesment by tomography
    angiotomography: Varicose and conadic Patency

    Full Information

    First Posted
    January 17, 2020
    Last Updated
    April 20, 2020
    Sponsor
    Hospital de Clínicas Dr. Manuel Quintela
    Collaborators
    University of the Republic, Uruguay, Centro Cardiovascular Universitario, Centro Hospitalario Pereyra Rossell
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT04358497
    Brief Title
    Endovascular Versus Medical Treatment for the Pelvic Congestion Syndrome
    Acronym
    ENDPCS
    Official Title
    Endovascular Versus Medical Treatment for the Pelvic Congestion Syndrome
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    October 1, 2020 (Anticipated)
    Primary Completion Date
    July 31, 2022 (Anticipated)
    Study Completion Date
    October 1, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Hospital de Clínicas Dr. Manuel Quintela
    Collaborators
    University of the Republic, Uruguay, Centro Cardiovascular Universitario, Centro Hospitalario Pereyra Rossell

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    Yes
    Product Manufactured in and Exported from the U.S.
    Yes
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    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.
    Detailed Description
    Pelvic congestion syndrome (PCS) is a recognized and frequent cause of Chronic Pelvic Pain (10% to 30%). It is defined as the presence of chronic symptoms, which may include pelvic pain, perineal heaviness, urinary urgency and postcoital pain, caused by reflux and / or obstruction of the gonadic and / or pelvic veins, and that may be associated with vulvar, perineal and lower limbs varicose veins. There is no standard approach to managing PCS. According to expert recommendations, therapies should be individualized according to the patient's symptoms and needs. Medical treatment options include progestagens, danazol, combined oral hormonal contraceptives, phlebotonics such as hisperidine-added diosmin, non-steroidal anti-inflammatory drugs and gonadotropin-releasing hormone (GnRH) agonists Currently, the only accepted chronic medical treatment is the association of non-steroidal and phlebotonic anti-inflammatories, but they have shown a poor symptomatic benefit in reducing pain. Surgical treatment has evolved over time mainly in the hands of laparoscopic techniques, currently the endovascular option is the most widely accepted for presenting excellent long-term results with abolition of pain in up to 90% at 2 years. HYPOTHESIS Endovascular treatment of pelvic congestion syndrome is better in terms of pain control and quality of life compared to drug treatment. General objective 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. Specific objectives • Compare pain in patients undergoing endovascular treatment with the best medical treatment. Evaluate the persistence of pelvic varices in patients undergoing endovascular treatment of SCP. Compare the Female Sexual Satisfaction Index in both groups.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Pelvic Congestive Syndrome, Pelvic Varices, Venous Disease
    Keywords
    pelvic congestion syndrome, sclerosis, coil embolization

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Model Description
    Blind randomized clinical trial designed to compare the efficacy and safety of endovascular treatment of Pelvic congestion syndrome.
    Masking
    ParticipantCare ProviderOutcomes Assessor
    Masking Description
    Phlebography will be performed to both groups. On the experimental group, the treatment of the pelvic congestion will be performed, while the procedure will be stopped on the control group. Neither the patient or the reference gynecologist will be informed if the treatment took place.
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Interventional treatment plus best chronic medical treatment
    Arm Type
    Experimental
    Arm Description
    Sandwich embolization ( 2% polidocanol + Coils) Diosmin hisperidin 1g twice a day for 6 months Ibuprofen 500mg 3 times a day for 6 months
    Arm Title
    Best chronic medical treatment alone
    Arm Type
    Active Comparator
    Arm Description
    Diosmin hisperidin 1g twice a day for 6 months Ibuprofen 500mg 3 times a day for 6 months
    Intervention Type
    Device
    Intervention Name(s)
    Medtronic® Concerto® detachable coil system
    Other Intervention Name(s)
    concerto detachable coil system
    Intervention Description
    coil embolization of the reflux pathways
    Intervention Type
    Procedure
    Intervention Name(s)
    sclerosis
    Other Intervention Name(s)
    Foam sclerosis with polidocanol 2%
    Intervention Description
    Pelvic varices sclerosis with polidocanol foam
    Intervention Type
    Drug
    Intervention Name(s)
    Diosmin / Hesperidin
    Other Intervention Name(s)
    daflon
    Intervention Description
    Best chronic medial treatment
    Intervention Type
    Drug
    Intervention Name(s)
    Ibuprofen 400 mg
    Other Intervention Name(s)
    Nsaid
    Intervention Description
    NSAID treatment
    Primary Outcome Measure Information:
    Title
    visual analogue scale (VAS)
    Description
    Pain assessment 1-10 from no pain to severe
    Time Frame
    30 days
    Title
    visual analogue scale (VAS)
    Description
    Pain assessment 1-10 from no pain to severe
    Time Frame
    3 months
    Title
    Lattinen index
    Description
    chronic pain assessment 2-22 from low to high
    Time Frame
    30 days
    Title
    Lattinen index
    Description
    chronic pain assessment 2-22 from low to high
    Time Frame
    3 months
    Title
    McGill Pain Questionnaire
    Description
    subjective pain experience assessment
    Time Frame
    30 days
    Title
    McGill Pain Questionnaire
    Description
    subjective pain experience assessment
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    Female sexual function index
    Description
    questionnaire that assesses different domains of sexual function. 0-48 from no sexual distress to high level of sexual distress
    Time Frame
    30 days
    Title
    Female sexual function index
    Description
    questionnaire that assesses different domains of sexual function. . 0-48 from no sexual distress to high level of sexual distress
    Time Frame
    3 months
    Title
    varicose and reflux persistance by transabdominal duplex scan
    Description
    transabdominal duplex scan: varicose permeability, prescience of gonadic or iliac reflux
    Time Frame
    30 days
    Title
    varicose and reflux persistance by transabdominal duplex scan
    Description
    transabdominal duplex scan: varicose permeability, prescience of gonadic or iliac reflux
    Time Frame
    3 months
    Title
    varicose and reflux persistance by transvaginal duplex scan
    Description
    transabdominal duplex scan: varicose permeability, prescience of gonadic or iliac reflux
    Time Frame
    3 months
    Title
    varicose persistance assesment by tomography
    Description
    angiotomography: Varicose and conadic Patency
    Time Frame
    3 months
    Other Pre-specified Outcome Measures:
    Title
    Deep venous thrombosis by duplex ultrasound
    Description
    Deep venous thrombosis of the iliac or femoral axis will be reported
    Time Frame
    30 days

    10. Eligibility

    Sex
    Female
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    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.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Sebastian Sarutte, VS
    Phone
    +59899533449
    Email
    ssarutte1@hotmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Mauricio Volpi, VS
    Phone
    +59899605556
    Email
    mavolpi@yahoo.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Sebastian Sarutte, VS
    Organizational Affiliation
    Centro Cardiovascular Universitario
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    De-identified data base for all variables will be available for researchers
    IPD Sharing Time Frame
    From April 2022 to april 2024
    IPD Sharing Access Criteria
    Data will be shared on request, after signing a discretion agreement.

    Learn more about this trial

    Endovascular Versus Medical Treatment for the Pelvic Congestion Syndrome

    We'll reach out to this number within 24 hrs