ClinicalTrials.gg
Status unknownNCT02033863OCCLUDE-IUpdated Jun 24, 2015

Evaluation of PerformanCe of the Peripheral EOS in the Treatment of Varicocele or Pelvic Congestion SynDromE

An observational study in Varicocele and Pelvic Congestion Syndrome, sponsored by ArtVentive Medical Group, Inc.. Status unknown at 3 sites in 3 countries. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2015-06-24.

Sponsored by ArtVentive Medical Group, Inc. · Observational

The sponsor has not verified this record recently (last verified Jun 2015), so the status shown — last known as Enrolling by invitation — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
40
Ages
18 Years to 75 Years
Sex
All
01

Study summary

To collect confirmatory data in support of the safety and performance of the ArtVentive Medical Group Endoluminal Occlusion System.

Read the detailed description

Prospective, non-randomized, multi-center confirmatory observational study for the treatment of subjects with the need for vascular occlusion for the following conditions:

  1. Cohort A: Varicocele arising from the spermatic vein(s) and pampiniform plexus, with or without concomitant diagnosis of infertility or subfertility
  2. Cohort B: Pelvic varices in females for the treatment of pelvic congestion syndrome (e.g., pelvic venous incompetence).
02

Conditions studied

  • Varicocele
  • Pelvic Congestion Syndrome

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Keywords

  • Varicocele
  • Pelvic Congestion Syndrome
  • Pelvic Venous Incompetence
  • Ovarian Varices
03

In context

Varicocele

53 studies on the registry are indexed under Varicocele; 15 are open to participants now.

This study's planned enrollment of 40 is below the median of 119 across 17 observational studies indexed under Varicocele.

Browse Varicocele studies →

Lead sponsor

ArtVentive Medical Group, Inc. is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Subjects requiring permanent occlusion of the peripheral vessels for the following conditions:

  1. Cohort A: Varicocele arising from the spermatic vein(s) and pampiniform plexus, with or without concomitant diagnosis of infertility or subfertility.
  2. Cohort B: Pelvic varices in females for the treatment of pelvic congestion syndrome (e.g., pelvic venous incompetence).

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Subjects aged ≥18 to ≤75 years.
  2. Subject with target vessels of 3.0 mm to 12.0 mm in diameter.
  3. Subject having indications to undergo embolotherapy consistent with clinical and pre-procedural angiographic assessment for spermatic vein origin varicocele (unilateral and/or bilateral) or pelvic congestion syndrome (pelvic venous incompetence).
  4. Subject is able and willing to comply with site standard medical follow-up, including one month follow-up visit.
  5. Subject or subject's legal representative have been informed of the nature of the study, agrees to participate and has signed the consent form.

Exclusion criteria

Exclusion Criteria:

  1. Subject has an active systemic infection.
  2. Subject has a known allergy to iodinated contrast for which they cannot be adequately premedicated.
  3. Subject has history of stroke within the prior 6 months.
  4. Subject has history of myocardial infarction with the prior 3 months.
  5. Subject has acute or chronic renal disease (e.g., as measured by a serum creatinine of >2.5 mg/dL or >220 umol/L), or on dialysis.
  6. Subject has a known coagulopathy or has a bleeding diatheses, thrombocytopenia with count less than 100,000/microliter, or >1.5.
  7. Co-morbid conditions that place the subject at an unacceptable surgical risk (e.g., severe , hepatic failure, cardiac disease, disorders or conditions of severe ).
  8. Subjects in whom venography or arteriography is .
  9. Subjects with known or contraindication to nickel or nitinol.
  10. Subject has a less than one year .
  11. Subject is pregnant or breastfeeding.
  12. Subject with endometriosis or other ovarian / uterine pathology with adhesions that would interfere with the endpoints of this study.
  13. Subject with previous pelvic surgical intervention or embolotherapy for varicocele or ovarian varices that would interfere with the endpoints of this study, including but not limited to, recurrent varicocele or ovarian varices.
  14. Any clinical evidence that the investigator feels would place the subject at increased risk with the deployment of the device.
  15. Subject has planned concomitant procedure at the time of the embolization (e.g., coil embolization, etc.).
  16. Subject is participating in another study of a device, medication, biologic, or other agent within 30 days or could, in the opinion of the investigator, impact the results of this study.
  17. Subject has other medical, social or psychological problems that in the opinion of the investigator would preclude them from receiving this treatment and the procedures and or participating in evaluations pre- and post-treatment.
Terms in these criteria, in plain language(8)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

INR, PT and aPTT (clotting tests)

Blood tests of how long blood takes to clot. The INR is the prothrombin time (PT) put on a common scale; about 1 is usual for someone not taking a blood thinner.

Criteria often make an exception for people on a blood thinner such as warfarin, whose INR is raised on purpose.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
40 participants (estimated)
Target follow-up
30 Days
Patient registry
Yes

Groups and cohorts

  • Cohort A

    Varicocele arising from the spermatic vein(s) and pampiniform plexus, with or without concomitant diagnosis of infertility or subfertility

  • Cohort B

    Pelvic varices in females for the treatment of pelvic congestion syndrome (e.g., pelvic venous incompetence).

06

What researchers measure

Primary outcomes

  1. Safety

    Composite of new-onset major device-related adverse event(s) including device embolization beyond targeted treatment area (not therapeutic indication of embolization), need for emergency surgical intervention of the target vessel, or distal embolization (non-device embolization, e.g., particulate matter / plaque distal to the device) at 30 days.

    Time frame: Acute & 30 days

Secondary outcomes

  1. Pain

    Reduction of pain.

    Time frame: Acute & 30 days

  2. Recurrent varices

    Recurrence of varices requiring repeat embolizations within 30 days.

    Time frame: 30 days

  3. Occlusion

    Sustained occlusion at 30 days follow-up.

    Time frame: 30 days

07

Study locations

3 sites
  • UZ Leuven
    Leuven, Belgium
  • University Hospital No4
    Lubin, Poland
  • Ospedale Regionale di Lugano
    Lugano, Switzerland
08

References and documents

Publications

  • Venbrux AC, Rudakov L, Plass A, Emmert MY, Ebner A. A new occlusion device: application of the ArtVentive endoluminal occlusion system (EOS)--first in human clinical trial. Cardiovasc Intervent Radiol. 2014 Feb;37(1):85-93. doi: 10.1007/s00270-013-0626-y. Epub 2013 May 24. PubMed 23703667 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02033863
Lead sponsor
ArtVentive Medical Group, Inc.
Responsible party
Sponsor
First posted
Jan 13, 2014
Start date
Jul 2014
Primary completion
Dec 2015 (estimated)
Completion
Jan 2016 (estimated)
Last update
Jun 24, 2015

Study contacts

Geert Maleux, MD
principal investigator · UZ Leuven, Belgium

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2015. You cannot join it, but the record below documents what was studied.

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