Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02037113 · ClinicalTrials.gov registry record

Outcomes of Femoro-popliteal Disease After Stent Deployment Under Intravascular Ultrasound Guidance

A clinical trial, sponsored by Texas Tech University Health Sciences Center.

Terminated
Registry status
8
Enrollment target

NCT02037113: Clinical Trial study, sponsored by Texas Tech University Health Sciences Center.

NCT02037113 is a clinical trial that was terminated before completion, run by Texas Tech University Health Sciences Center. The registered enrollment target is 8 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02037113 was terminated before completion, sponsored by Texas Tech University Health Sciences Center.

TERMINATED
Registry status
8 participants
Enrollment target

Study Summary

This is a prospective, single-center study. The patients with peripheral arterial disease who underwent abdominal aortograms with runoff (which are arteriograms of the lower abdominal aorta and arteries in the legs) and Intravascular Ultrasound after stent deployment will be enrolled in the study. All patients who participated in the study will be treated according to standard of care. HYPOTHESIS The higher degree of plaque burden on landing zone has an effect on restenosis on peripheral artery intervention. SPECIFIC AIMS 1. To determine intravascular ultrasound parameters of stent deployment and outcomes of Femoro-popliteal Disease 2. To determine clinical risk factors and outcomes of Femoro-popliteal Disease 3. To obtain data that will eventually support development of a predictive model for ISR in Femoro-popliteal Disease METHODOLOGY Visit 1: After consent is given The subject will receive standard follow-up care. A member of the research team will collect information such as the subject's age, sex, ethnicity, and medical information from the subject's medical record. Visits 2-5: 1 day after enrollment, and at months 3 (+- 2 weeks), 6 (+- 2 weeks), and 12 (+- 2 weeks) The subject will complete standard follow-up appointment at TTUHSC. This may include a Doppler ultrasound. A member of the research team will record information such as medications, ultrasounds, and need for additional care related to the subject's stent. The subject will complete the questionnaire on leg pain and mobility.

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2014-01
Est. Completion 2016-08

Why NCT02037113 stopped before completion

NCT02037113 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 8 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT02037113 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02037113 about?

NCT02037113 is a clinical study titled "Outcomes of Femoro-popliteal Disease After Stent Deployment Under Intravascular Ultrasound Guidance". This is a prospective, single-center study. The patients with peripheral arterial disease who underwent abdominal aortograms with runoff (which are arteriograms of the lower abdominal aorta and arteries in the legs) and Intravascular Ultrasound after stent deployment will be enrolled in the study. A...

What is the current status of trial NCT02037113?

This trial is currently terminated. The enrollment target is 8 participants. The study started on 2014-01. Estimated completion is 2016-08.

Who is sponsoring clinical trial NCT02037113?

This trial is sponsored by Texas Tech University Health Sciences Center, which has 76 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02037113, the US trial registry maintained by the National Library of Medicine. NCT02037113 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.