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RECRUITING Phase 2

Reducing Frailty for Older Cancer Survivors Using Supplements II

NCT06068543 · View on ClinicalTrials.gov ↗

Study Summary

This study is a two-arm placebo controlled randomized clinical trial, to assess the effect of a 12-week EGCG intervention on physical frailty compared to placebo in pre-frail older cancer survivors.

Conditions Studied

Interventions

  • DRUG Epigallocatechin-3-Gallate (EGCG)
  • DRUG Microcrystalline cellulose (MCC)
  • DIETARY_SUPPLEMENT Ascorbic Acid (Vitamin C)

Study Locations (1)

New York

  • University of Rochester — Rochester

Trial Details

FieldValue
Enrollment Target 118 participants
Start Date 2024-10-25
Est. Completion 2030-12-31
Phase Phase 2

Sponsor

University of Rochester

437 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06068543

The ClinicalTrials.gov registry entry for NCT06068543 describes a study currently listed as recruiting. 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 118 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Rochester, which has 437 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Inflammation appearing as the primary indexed condition, and to 3 interventions — of which Epigallocatechin-3-Gallate (EGCG) 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: NCT06068543 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 NCT06068543 about?

NCT06068543 is a clinical study titled "Reducing Frailty for Older Cancer Survivors Using Supplements II". This study is a two-arm placebo controlled randomized clinical trial, to assess the effect of a 12-week EGCG intervention on physical frailty compared to placebo in pre-frail older cancer survivors.

What is the current status of trial NCT06068543?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 118 participants. The study started on 2024-10-25. Estimated completion is 2030-12-31.

What conditions does trial NCT06068543 study?

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

What interventions are being tested in trial NCT06068543?

The interventions under investigation include: Epigallocatechin-3-Gallate (EGCG) (DRUG), Microcrystalline cellulose (MCC) (DRUG), Ascorbic Acid (Vitamin C) (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06068543?

This trial is sponsored by University of Rochester, which has 437 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06068543 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