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

NCT01534910 · ClinicalTrials.gov registry record · Phase 4

Effect of Aged Garlic Extract on Atherosclerosis

A Phase 4 study, sponsored by Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center.

Completed
Registry status
Phase 4
Development phase
65
Enrollment target

NCT01534910: Completed Phase 4 study, sponsored by Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center.

NCT01534910 is a Phase 4 study that has completed, run by Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center. The registered enrollment target is 65 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01534910, a Phase 4 study, has completed, sponsored by Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center.

COMPLETED
Registry status
Phase 4
Development phase
65 participants
Enrollment target

Study Summary

The investigators will be assessing the effect of Aged Garlic Extract on the coronary arteries. The investigators will enroll patients in a double blind study, where half the patients will receive placebo, and have the patients undergo a series of tests of plaque (CT scan of the heart, carotid ultrasound) and follow the patients on the drug or placebo and then repeat the tests and blood work at the end of one year. The investigators will assess if being on aged garlic extract adds any benefit to plaque in the coronary or neck arteries. The investigators will also assess the effect of aged garlic extract on markers of inflammation. Patients will receive free drug, free testing and be compensated, and learn more about their heart and neck arteries. if successful, more patients can use this drug to benefit their health. The harms include the radiation from the CT scan and the medication, which has mild side effects.

Primary Outcome

we will measure low attenuation plaque at baseline (in volume) and then again at 1 year. we will assess if there is a reduction in low attenuation plaque volume (percent change from baseline), defined as \[followup-baseline\]/baseline x100%. Baseline was time zero, followup CT scan was 1 year.

Interventions

  • DRUG placebo
  • DRUG aged garlic extract

Trial Details

FieldValue
Enrollment Target 65 participants
Start Date 2012-05
Est. Completion 2014-12
Phase Phase 4

What the finished NCT01534910 record still lists

NCT01534910 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.

NCT01534910 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01534910 about?

NCT01534910 is a clinical study titled "Effect of Aged Garlic Extract on Atherosclerosis". The investigators will be assessing the effect of Aged Garlic Extract on the coronary arteries. The investigators will enroll patients in a double blind study, where half the patients will receive placebo, and have the patients undergo a series of tests of plaque (CT scan of the heart, carotid ultra...

What is the current status of trial NCT01534910?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 65 participants. The study started on 2012-05. Estimated completion is 2014-12.

What interventions are being tested in trial NCT01534910?

The interventions under investigation include: placebo (DRUG), aged garlic extract (DRUG).

Who is sponsoring clinical trial NCT01534910?

This trial is sponsored by Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, which has 55 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01534910's enrollment target sits among peer trials

65 1091st of 2000 higher than 903 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

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

Similar enrollment target

  • NCT03366116 · 65 participants · Phase 1

    5-aza-4'-Thio-2'-Deoxycytidine (Aza-TdC) in People With Advanced Solid Tumors

  • NCT03603730 · 65 participants · NA

    Vagal Nerve Stimulation for Functional Dyspepsia and Gastroparesis

  • NCT03796559 · 65 participants · NA

    Magseed Enabled Long-Term Localization of Axillary Lymph Nodes

  • NCT03993106 · 65 participants · Phase 2

    A Study of sEphB4-HSA in Kaposi Sarcoma

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 NCT01534910, the US trial registry maintained by the National Library of Medicine. NCT01534910 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.