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Clinical Trials/NCT01699581
NCT01699581
Terminated
Phase 2

Assessment of Impact Nutritional Program During Autologous Stem Cell Transplant

Greg Monohan1 site in 1 country35 target enrollmentSeptember 2012

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Hodgkin's Lymphoma
Sponsor
Greg Monohan
Enrollment
35
Locations
1
Primary Endpoint
Hospital length of stay
Status
Terminated
Last Updated
9 years ago

Overview

Brief Summary

Nestle Impact has shown efficacy in multiple surgical trials in relation to improving hospital length of stay and infection rate. 1 dose of Nestle Impact Advanced Recovery will be taken orally three times a day beginning on the morning following stem cell transplant and will continue until the day of hospital discharge.

Registry
clinicaltrials.gov
Start Date
September 2012
End Date
October 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Greg Monohan
Responsible Party
Sponsor Investigator
Principal Investigator

Greg Monohan

Principal Investigator

University of Kentucky

Eligibility Criteria

Inclusion Criteria

  • Patients receiving an autologous stem cell transplant using the preparative regimens of BEAM (Carmustine, Etoposide, Cytarabine, Melphalan), Melphalan 140mg/m2, or Melphalan 200mg/m2
  • Any prior diet or supplement will be allowed.
  • Age \>18 years.
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria

  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to Nestle Impact including fish oil.

Outcomes

Primary Outcomes

Hospital length of stay

Time Frame: Particpants will be followed for 14 days, the average length of time from stem cell infusion until dischcarge

Days to engraftment

Time Frame: Particpants will be followed for 14 days, the average length of time from stem cell infusion until dischcarge

Study Sites (1)

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