跳至主要内容
临床试验/NCT06888024
NCT06888024招募中不适用

Pelvic Vein Quantitative Flow Characterization Using 2D and 4D Flow MRI

Ningcheng Peter Li2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2025年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
15
试验地点
2
主要终点
Flow Volume

研究概览

简要总结

The purpose of the study is to quantitatively characterize the flow in the pelvic venous structures using 2D and 4D flow MRI with the objective of establishing physiologic and pathologic parameters for downstream computational fluid dynamics analysis.

Arm 1: To establish the baseline flow characteristics of the iliac veins in patients with no imaging evidence of iliac venous disease.

Arm 2: To assess the flow characteristics of the iliac veins in patients with left iliac vein compression syndrome (a.k.a. May-Thurner syndrome).

Arm 3: To assess the flow characteristics of the iliac veins in patients status post iliac stent placement.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Arm 1: Inclusion Criteria:
  • •No self-reported history of pelvic or iliac venous disease or associated symptoms

排除标准

  • •History of pelvic or iliac venous disease or intervention
  • •Contraindication to MRI examination
  • •Prisoners
  • •Subjects ≤ 18 years of age
  • •Pregnant women
  • •Adults unable to provide informed consent
  • •Arm 2: Inclusion Criteria:
  • •Clinical symptoms or imaging findings compatible with left iliac vein compression syndrome
  • •Exclusion Criteria:
  • •History of pelvic or iliac venous intervention
  • •Contraindication to MRI examination
  • •Prisoners
  • •Subjects ≤ 18 years of age
  • •Pregnant women
  • •Adults unable to provide informed consent
  • •Arm 3: Inclusion Criteria:
  • •History of left iliac vein stent placement
  • •Exclusion Criteria:
  • •Contraindication to MRI examination
  • •Prisoners
  • •Subjects ≤ 18 years of age
  • •Pregnant women
  • •Adults unable to provide informed consent

研究组 & 干预措施

Patients with left iliac vein compression syndrome (a.k.a. May-Thurner syndrome).

Experimental

Patients with prior imaging evidence of left common iliac vein compression syndrome to undergo 2D and 4D flow MRI without contrast administration

干预措施: non-contrast enhanced abdomen and pelvis MRI (Procedure)

Patients status post iliac stent placement

Experimental

Patients with a history of iliac stent placement to undergo 2D and 4D flow MRI without contrast administration

干预措施: non-contrast enhanced abdomen and pelvis MRI (Procedure)

Patients with no imaging evidence of iliac venous disease

Experimental

Healthy volunteers with no self-reported history or prior imaging evidence of pelvic venous disease or associated symptoms to undergo 2D and 4D flow MRI without contrast administration

干预措施: non-contrast enhanced abdomen and pelvis MRI (Procedure)

结局指标

主要结局

Flow Volume

时间窗: At Enrollment

Flow volume in the iliac veins calculated based on the 2D and 4D flow MRI obtained.

12-month primary patency rate

时间窗: 12 Months

Freedom from occlusion of the stented segment; Freedom from restenosis \>=50%; and Freedom from clinically-driven target lesion revascularization

次要结局

  • Quality-of-life measures(Baseline to 6 Months, 12 Months, 24 Months, 36 Months)
  • Flow Velocity Profile(At Enrollment)
  • Quality-of-life measure: Venous clinical severity score (VCSS)(Baseline to 6 Months, 12 Months, 24 Months, 36 Months)
  • Technical success(Index Procedure)
  • Target vessel revascularization(30 days, 6 months, 12 months, 24 months, 36 months)
  • Target lesion revascularization(30 days, 6 months, 12 months, 24 months, 36 months)
  • Major adverse events(6 Months, 12 Months, 24 Months, 36 Months)
  • Clinical-etiologic-anatomic-pathophysiologic clinical score (CEAP)(Baseline to 6 Months, 12 Months, 24 Months, 36 Months)
  • Primary Patency(24 Months, 36 Months)
  • Stent integrity(30 Days, 12 Months, 24 Months, 36 Months)

研究者

发起方
Ningcheng Peter Li
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ningcheng Peter Li

Principal Investigator

University of Massachusetts, Worcester

研究点 (2)

Loading locations...

相似试验