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

NCT00467220 · ClinicalTrials.gov registry record · NA

Effect of Daily Calorie or Alternate-day Calorie Reductions on Risk for Cardiovascular Disease and Cancer

A NA study of Moderately Overweight Individuals, sponsored by University of California, San Francisco.

Completed
Registry status
NA
Development phase
24
Enrollment target
1
Study location

NCT00467220: Completed NA study of Moderately Overweight Individuals, sponsored by University of California, San Francisco.

NCT00467220 is a NA study of Moderately Overweight Individuals that has completed, run by University of California, San Francisco. The registered enrollment target is 24 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00467220, a NA study of Moderately Overweight Individuals, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
NA
Development phase
24 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to examine and compare the effects of alternate-day reductions in calorie intake or daily calorie restriction on the risk for cardiovascular disease and cancer.

Primary Outcome

Parameters measured will include adipose tissue dynamics (triglyceride turnover, lipolysis, de novo lipogenesis, adipose cell proliferation), adipose tissue morphology (cell size and number), adipose tissue hormone levels (adiponectin, leptin), skin turnover (keratin dynamics), T-lymphocyte proliferation, as well as plasma lipid and lipoprotein, homocysteine, and C-reactive protein levels.

Interventions

  • BEHAVIORAL calorie restriction

Study Locations (1)

California

  • San Francisco General Hospital - San Francisco

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2007-04
Est. Completion 2015-12-17
Phase NA

What the finished NCT00467220 record still lists

NCT00467220 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Moderately Overweight Individuals appearing as the primary indexed condition, and to 1 intervention - of which calorie restriction is the first listed.

NCT00467220 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT00467220 about?

NCT00467220 is a clinical study titled "Effect of Daily Calorie or Alternate-day Calorie Reductions on Risk for Cardiovascular Disease and Cancer". The purpose of this study is to examine and compare the effects of alternate-day reductions in calorie intake or daily calorie restriction on the risk for cardiovascular disease and cancer.

What is the current status of trial NCT00467220?

This trial is currently completed. It is a NA study. The enrollment target is 24 participants. The study started on 2007-04. Estimated completion is 2015-12-17.

What conditions does trial NCT00467220 study?

This clinical trial studies the following conditions: Moderately Overweight Individuals.

What interventions are being tested in trial NCT00467220?

The interventions under investigation include: calorie restriction (BEHAVIORAL).

Who is sponsoring clinical trial NCT00467220?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00467220 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT00467220's enrollment target sits among peer trials

24 1736th of 2000 higher than 246 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00467220, the US trial registry maintained by the National Library of Medicine. NCT00467220 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.