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

NCT03493204 · ClinicalTrials.gov registry record · NA

Tackling 30-day Readmissions in Patients With Cirrhosis: The SALTYFOOD Trial

A NA study, sponsored by University of Michigan.

Completed
Registry status
NA
Development phase
44
Enrollment target

NCT03493204: Completed NA study, sponsored by University of Michigan.

NCT03493204 is a NA study that has completed, run by University of Michigan. The registered enrollment target is 44 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03493204, a NA study, has completed, sponsored by University of Michigan.

COMPLETED
Registry status
NA
Development phase
44 participants
Enrollment target

Study Summary

The purpose of this study is to determine the feasibility of a home meal delivery program for patients with cirrhosis and ascites and to determine the effectiveness of a salt-restricted (2 gram sodium) meal delivery program in reducing the need for therapeutic paracenteses and/or all-cause re-admissions for these patients. Many patients with cirrhosis don't have enough nutrients in the body and are frail and these meals may help them maintain a good diet and lead to improved quality of life.

Primary Outcome

Number of paracenteses

Interventions

  • OTHER Meal delivery
  • OTHER Standard pamphlet with Dietary Advice

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2018-04-24
Est. Completion 2019-08-19
Phase NA
University of Michigan

1,327 total trials

What the finished NCT03493204 record still lists

NCT03493204 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which Meal delivery is the first listed.

NCT03493204 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03493204 about?

NCT03493204 is a clinical study titled "Tackling 30-day Readmissions in Patients With Cirrhosis: The SALTYFOOD Trial". The purpose of this study is to determine the feasibility of a home meal delivery program for patients with cirrhosis and ascites and to determine the effectiveness of a salt-restricted (2 gram sodium) meal delivery program in reducing the need for therapeutic paracenteses and/or all-cause re-admiss...

What is the current status of trial NCT03493204?

This trial is currently completed. It is a NA study. The enrollment target is 44 participants. The study started on 2018-04-24. Estimated completion is 2019-08-19.

What interventions are being tested in trial NCT03493204?

The interventions under investigation include: Meal delivery (OTHER), Standard pamphlet with Dietary Advice (OTHER).

Who is sponsoring clinical trial NCT03493204?

This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03493204's enrollment target sits among peer trials

44 1423rd of 2000 higher than 566 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

  • NCT02323945 · 44 participants · NA

    Effects of Breathing Mild Bouts of Low Oxygen on Limb Mobility After Spinal Injury

  • NCT03093909 · 44 participants · Phase 1

    Study of Aerosol Gemcitabine in Patients With Solid Tumors and Pulmonary Metastases

  • NCT03104491 · 44 participants · Phase 1

    Inotuzumab Ozogamicin Post-Transplant For Acute Lymphocytic Leukemia

  • NCT03781765 · 44 participants · Phase 4

    Stimulant vs. Non-stimulant Treatments and Reward Processing in Drug-naive Youth at SUD Risk

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 NCT03493204, the US trial registry maintained by the National Library of Medicine. NCT03493204 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.