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NCT05359848 · ClinicalTrials.gov registry record · NA

A Pilot, Feasibility Study of Intermittent Caloric Restriction Plus Plant-based Diet in Cancer Patients Receiving Chemotherapy

A NA study of Medical Oncology and Integrative Oncology, sponsored by State University of New York at Buffalo.

Recruiting
Registry status
NA
Development phase
30
Enrollment target
2
Study locations

NCT05359848: Recruiting NA study of Medical Oncology and Integrative Oncology, sponsored by State University of New York at Buffalo.

NCT05359848 is a NA study of Medical Oncology and Integrative Oncology that is actively recruiting participants, run by State University of New York at Buffalo. The registered enrollment target is 30 participants, below the 253-participant average among 3 other Medical Oncology trials with a reported enrollment target (88% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05359848, a NA study of Medical Oncology and Integrative Oncology, is actively recruiting participants, sponsored by State University of New York at Buffalo.

RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target
2
Study locations

Study Summary

Caloric restriction may alter the response to chemotherapy induced stress response and enhance its antitumor effect. This study intends to use an intermitted caloric restriction protocol with alternate days before the chemotherapy administration to enhance the cytotoxic effect generated by standard treatment of cancer.

Primary Outcome

enrollment rate

Interventions

  • OTHER Diet

Study Locations (2)

New York

  • University at Buffalo / Great Lakes Cancer Care - Buffalo
  • University at Buffalo / Great Lakes Cancer Care - Buffalo

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2022-04-15
Est. Completion 2027-06-01
Phase NA

What NCT05359848 shows while recruiting

NCT05359848 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 253-participant average among 3 other Medical Oncology trials with a reported enrollment target (88% lower).

The record links to 3 conditions, with Medical Oncology appearing as the primary indexed condition, and to 1 intervention - of which Diet is the first listed.

NCT05359848 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT05359848 about?

NCT05359848 is a clinical study titled "A Pilot, Feasibility Study of Intermittent Caloric Restriction Plus Plant-based Diet in Cancer Patients Receiving Chemotherapy". Caloric restriction may alter the response to chemotherapy induced stress response and enhance its antitumor effect. This study intends to use an intermitted caloric restriction protocol with alternate days before the chemotherapy administration to enhance the cytotoxic effect generated by standard ...

What is the current status of trial NCT05359848?

This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2022-04-15. Estimated completion is 2027-06-01.

What conditions does trial NCT05359848 study?

This clinical trial studies the following conditions: Medical Oncology, Integrative Oncology, Medical Nutrition Therapy.

What interventions are being tested in trial NCT05359848?

The interventions under investigation include: Diet (OTHER).

Who is sponsoring clinical trial NCT05359848?

This trial is sponsored by State University of New York at Buffalo, which has 243 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05359848 being conducted?

This trial has 2 study locations across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT05359848, the US trial registry maintained by the National Library of Medicine. NCT05359848 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.