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COMPLETED Phase 2

Efficacy and Safety Study of Lipid-Lowering Effects of XueZhiKang (XZK) in Patients With Hyperlipidemia

NCT01327014 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to demonstrate the efficacy of XueZhiKang to improve plasma lipid profile, as compared to placebo, in outpatients with hyperlipidemia.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG XueZhiKang (XZK), a botanic product with multiple components

Study Locations (13)

Texas

  • Osvaldo Brusco, MD — Corpus Christi
  • Clinical Trial Network — Houston

Shanghai Municipality

  • Shanghai Ruijin Hospital — Shanghai
  • Shanghai First People's Hospital — Shanghai

California

  • Robert Karns, MD A Medical Corporation — Beverly Hills

Florida

  • Jellinger and Lerman, MD — Hollywood

Kansas

  • Department of Internal Medicine, University of Kansas Medical Center — Kansas City

Kentucky

  • Harold E Bays, MD — Louisville

Ohio

  • Eli M Roth, MD — Cincinnati

Pennsylvania

  • Cardiovascular Medical Associates — Philadelphia

Trial Details

FieldValue
Enrollment Target 116 participants
Start Date 2011-04
Est. Completion 2012-12
Phase Phase 2

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01327014

The ClinicalTrials.gov registry entry for NCT01327014 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 116 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beijing Peking University WBL Biotech Co., which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Hyperlipidemia appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01327014 reports 13 study locations spanning 11 distinct geographic areas — top geographies include Texas, Shanghai Municipality, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01327014 about?

NCT01327014 is a clinical study titled "Efficacy and Safety Study of Lipid-Lowering Effects of XueZhiKang (XZK) in Patients With Hyperlipidemia". The purpose of this study is to demonstrate the efficacy of XueZhiKang to improve plasma lipid profile, as compared to placebo, in outpatients with hyperlipidemia.

What is the current status of trial NCT01327014?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 116 participants. The study started on 2011-04. Estimated completion is 2012-12.

What conditions does trial NCT01327014 study?

This clinical trial studies the following conditions: Hyperlipidemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01327014?

The interventions under investigation include: Placebo (DRUG), XueZhiKang (XZK), a botanic product with multiple components (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01327014?

This trial is sponsored by Beijing Peking University WBL Biotech Co., which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01327014 being conducted?

This trial has 13 study locations across California, Florida, Kansas, Kentucky, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial