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

NCT05565638 · ClinicalTrials.gov registry record · NA

PROFAST Intervention in Precursor Multiple Myeloma

A NA study, sponsored by Dana-Farber Cancer Institute.

Completed
Registry status
NA
Development phase
23
Enrollment target

NCT05565638: Completed NA study, sponsored by Dana-Farber Cancer Institute.

NCT05565638 is a NA study that has completed, run by Dana-Farber Cancer Institute. The registered enrollment target is 23 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05565638, a NA study, has completed, sponsored by Dana-Farber Cancer Institute.

COMPLETED
Registry status
NA
Development phase
23 participants
Enrollment target

Study Summary

This is a 4-month randomized trial of a prolonged nightly fasting intervention (PROFAST) in 40 overweight and obese individuals with monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), and smoldering waldenstrom macroglobulinemia (SWM). The purpose of this study is to understand if fasting for a prolonged period of time during the nighttime hours is a strategy to prevent overweight and obese individuals from developing blood cancer. Participants will be randomized into the following two groups: * Group A: PROFAST intervention for 4 months * Group B: Healthy Lifestyle Control group for 4 months

Primary Outcome

assessed via whole body DXA scans

Interventions

  • BEHAVIORAL Prolonged Fasting Intervention
  • BEHAVIORAL EDUCATION CONTROL

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2023-03-06
Est. Completion 2025-08-04
Phase NA
Dana-Farber Cancer Institute

781 total trials

What the finished NCT05565638 record still lists

NCT05565638 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 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 0 conditions, and to 2 interventions - of which Prolonged Fasting Intervention is the first listed.

NCT05565638 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05565638 about?

NCT05565638 is a clinical study titled "PROFAST Intervention in Precursor Multiple Myeloma". This is a 4-month randomized trial of a prolonged nightly fasting intervention (PROFAST) in 40 overweight and obese individuals with monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), and smoldering waldenstrom macroglobulinemia (SWM). The purpose of this s...

What is the current status of trial NCT05565638?

This trial is currently completed. It is a NA study. The enrollment target is 23 participants. The study started on 2023-03-06. Estimated completion is 2025-08-04.

What interventions are being tested in trial NCT05565638?

The interventions under investigation include: Prolonged Fasting Intervention (BEHAVIORAL), EDUCATION CONTROL (BEHAVIORAL).

Who is sponsoring clinical trial NCT05565638?

This trial is sponsored by Dana-Farber Cancer Institute, which has 781 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05565638's enrollment target sits among peer trials

23 1755th of 2000 higher than 245 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

  • NCT03616041 · 23 participants

    Capsule Endoscopy for Severe Hematochezia

  • NCT04348747 · 23 participants · Phase 2

    Dendritic Cell Vaccines Against Her2/Her3 and Pembrolizumab for the Treatment of Brain Metastasis From Triple Negative Breast Cancer or HER2+ Breast Cancer

  • NCT04587687 · 23 participants · Phase 2

    Brentuximab Vedotin and Bendamustine for the Treatment of Relapsed or Refractory Follicular Lymphoma

  • NCT04715022 · 23 participants · Phase 1

    Sympathetic-vascular Dysfunction in Obesity and Insulin Resistance (Vitamin C Study)

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05565638, the US trial registry maintained by the National Library of Medicine. NCT05565638 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.