Comparison of Intravascular Ultrasound With Venography in the Diagnosis and Treatment of Iliac Ve… (NCT03309969) | Clinical Trial Compass
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Comparison of Intravascular Ultrasound With Venography in the Diagnosis and Treatment of Iliac Vein Compression Syndrome
China50 participantsStarted 2017-10-30
Plain-language summary
The aim of this study is to compare intravascular ultrasound with venography in the diagnosis and treatment of iliac vein compression syndrome.
Who can participate
Age range
18 Years – 90 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age: 18 to 90 years
* Willing to participate in and sign the informed consent
* Patients with suspicious iliac vein stenosis or compression presented by preoperative magnetic resonance venography (MRV)
* Patent common femoral vein and/or femoral vein of the study leg
* Undergoing iliofemoral venography with the intend to treat potential iliac vein compression syndrome
Exclusion Criteria:
* Not providing informed consent
* Venous compression caused by pelvic tumors or fibroid uterus
* Previous stent implantation or venovenous bypass surgery of the study leg
* Known metal allergy precluding the possibility of stent implantation
* Known iodine allergy or severe renal insufficient function which are unsuitable for venography
* Pregnant or planning to be pregnant recently
* Acute deep vein thrombosis or tumor thrombus involving the study leg
* Know history of thrombophilia (e.g. protein C or S deficiency, anti-thrombin III deficiency, etc )
* Any concurrent disease, for example, heart failure, might make the patients unsuitable for surgery
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.