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

RECRUITING NA

Daily Amino Acid Supplementation for People With Parkinson's Disease

NCT07115563 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this clinical trial is to learn if a tailored amino acid supplement works to help adults living with Parkinson's disease to improve nutrition, metabolic function, body composition, and physical and mental function. The main questions it aims to answer are: Does the tailored amino acid supplement increase essential amino acids (nutritional status)? Does the tailored amino acid supplement increase an antioxidant (complex amino acid) and decrease an amino acid associated with oxidative stress? Does the tailored amino acid supplement improve physical and mental health compared to a placebo supplement? Researchers will compare the tailored amino acid supplement to a placebo (a look-alike substance that contains no active ingredients) to see if the tailored amino acid supplements work to support health for people with Parkinson's disease. Participants will: Take the tailored amino acid supplement or a placebo every day for 6 months, visit the lab at baseline, after 3 months, and after 6 months for fasting blood draws, body composition assessment, and physical and mental health testing and keep a diary of their food intake and supplement intake.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Control (placebo)
  • DIETARY_SUPPLEMENT Targeted Amino Acid Supplement

Study Locations (1)

Connecticut

  • University of Connecticut — Storrs

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2025-10-31
Est. Completion 2027-11
Phase NA

Sponsor

Cristina Colon-Semenza

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07115563

The ClinicalTrials.gov registry entry for NCT07115563 describes a study currently listed as recruiting. It is categorized as NA, 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 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cristina Colon-Semenza, 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 Parkinson Disease (PD) appearing as the primary indexed condition, and to 2 interventions — of which Control (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: NCT07115563 reports 1 study location spanning 1 distinct geographic area — top geographies include Connecticut. 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 NCT07115563 about?

NCT07115563 is a clinical study titled "Daily Amino Acid Supplementation for People With Parkinson's Disease". The goal of this clinical trial is to learn if a tailored amino acid supplement works to help adults living with Parkinson's disease to improve nutrition, metabolic function, body composition, and physical and mental function. The main questions it aims to answer are: Does the tailored amino acid s...

What is the current status of trial NCT07115563?

This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2025-10-31. Estimated completion is 2027-11.

What conditions does trial NCT07115563 study?

This clinical trial studies the following conditions: Parkinson Disease (PD). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07115563?

The interventions under investigation include: Control (placebo) (DIETARY_SUPPLEMENT), Targeted Amino Acid Supplement (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07115563?

This trial is sponsored by Cristina Colon-Semenza, 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 NCT07115563 being conducted?

This trial has 1 study location across Connecticut. 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