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COMPLETED Early Phase 1

The Effects of L-Tyrosine on 24 Hour Blood Pressure and Heart Rate in Parkinson's Disease

NCT02259049 · View on ClinicalTrials.gov ↗

Study Summary

The investigators are observing the effects 2,000 mg of L-tyrosine will have on 24 hour blood pressure fluctuations in individuals with Parkinson's disease.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Sugar Pill
  • DIETARY_SUPPLEMENT L-tyrosine

Study Locations (1)

New York

  • New York Institute of Technology — Old Westbury

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2014-10
Est. Completion 2015-09
Phase Early Phase 1

Sponsor

New York Institute of Technology

76 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02259049

The ClinicalTrials.gov registry entry for NCT02259049 describes a study currently listed as completed. It is categorized as Early Phase 1, 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 6 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is New York Institute of Technology, which has 76 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 Blood Pressure appearing as the primary indexed condition, and to 2 interventions — of which Sugar Pill 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: NCT02259049 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. 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 NCT02259049 about?

NCT02259049 is a clinical study titled "The Effects of L-Tyrosine on 24 Hour Blood Pressure and Heart Rate in Parkinson's Disease". The investigators are observing the effects 2,000 mg of L-tyrosine will have on 24 hour blood pressure fluctuations in individuals with Parkinson's disease.

What is the current status of trial NCT02259049?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 6 participants. The study started on 2014-10. Estimated completion is 2015-09.

What conditions does trial NCT02259049 study?

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

What interventions are being tested in trial NCT02259049?

The interventions under investigation include: Sugar Pill (DIETARY_SUPPLEMENT), L-tyrosine (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02259049?

This trial is sponsored by New York Institute of Technology, which has 76 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02259049 being conducted?

This trial has 1 study location across New York. 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