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NCT02919670 · ClinicalTrials.gov registry record · NA

A Study Evaluating a Proprietary Amino Acid Mixture (Enterade®) in Patients Receiving High-Dose Melphalan Conditioning Followed by Autologous Stem Cell Transplantation for Multiple Myeloma and Non-Hodgkin Lymphoma

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

Completed
Registry status
NA
Development phase
114
Enrollment target

NCT02919670: Completed NA study, sponsored by Dana-Farber Cancer Institute.

NCT02919670 is a NA study that has completed, run by Dana-Farber Cancer Institute. The registered enrollment target is 114 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02919670, a NA study, has completed, sponsored by Dana-Farber Cancer Institute.

COMPLETED
Registry status
NA
Development phase
114 participants
Enrollment target

Study Summary

This research study is evaluating Enterade, a supplement, as a possible treatment for the side effects caused by Stem Cell Transplant. The following interventions will be involved in this study: * Enterade plus standard supportive care * Placebo plus standard supportive care. The placebo will be a mixture of water, electrolytes, and sweetener.

Primary Outcome

Evaluation will made using Fisher's exact test. Among 99 participants who received some intervention

Interventions

  • DIETARY_SUPPLEMENT Placebo
  • DIETARY_SUPPLEMENT Enterade
  • OTHER Standard Supportive Care

Trial Details

FieldValue
Enrollment Target 114 participants
Start Date 2016-10
Est. Completion 2020-07
Phase NA
Dana-Farber Cancer Institute

781 total trials

What the finished NCT02919670 record still lists

NCT02919670 is an interventional study that assigns participants to a tested intervention. The registered 114 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT02919670 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02919670 about?

NCT02919670 is a clinical study titled "A Study Evaluating a Proprietary Amino Acid Mixture (Enterade®) in Patients Receiving High-Dose Melphalan Conditioning Followed by Autologous Stem Cell Transplantation for Multiple Myeloma and Non-Hodgkin Lymphoma". This research study is evaluating Enterade, a supplement, as a possible treatment for the side effects caused by Stem Cell Transplant. The following interventions will be involved in this study: * Enterade plus standard supportive care * Placebo plus standard supportive care. The placebo will be a...

What is the current status of trial NCT02919670?

This trial is currently completed. It is a NA study. The enrollment target is 114 participants. The study started on 2016-10. Estimated completion is 2020-07.

What interventions are being tested in trial NCT02919670?

The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Enterade (DIETARY_SUPPLEMENT), Standard Supportive Care (OTHER).

Who is sponsoring clinical trial NCT02919670?

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 NCT02919670's enrollment target sits among peer trials

114 811th of 2000 higher than 1,188 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

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Source: ClinicalTrials.gov NCT02919670, the US trial registry maintained by the National Library of Medicine. NCT02919670 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.