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CompletedNCT00575809Updated Jul 21, 2021

Incidence and Factors Associated With the Development and Severity of Oral Mucositis

An observational study in Peripheral Blood Stem Cell Transplantation, sponsored by The University of Texas Health Science Center at San Antonio. Completed at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-07-21.

Sponsored by The University of Texas Health Science Center at San Antonio · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
633
Ages
18 Years and older
Sex
All
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Study summary

Our study intends to evaluate prospectively the incidence and severity of oral mucositis in patients undergoing high-dose chemotherapy and hematopoietic stem cell transplantation, as well as to evaluate the potential influence of nutritional-, physical-, and transplant-related factors associated with the development of this complication and its grade of involvement.

Read the detailed description

Objective: Our study intends to evaluate prospectively the incidence and severity of oral mucositis in patients undergoing high-dose chemotherapy and hematopoietic stem cell transplantation, as well as to evaluate the potential influence of nutritional-, physical-, and transplant-related factors associated with the development of this complication and its grade of involvement.

Research plan: This is a prospective cohort study with an observational basis that involves all of the patients undergoing high-dose chemotherapy and peripheral blood stem cell transplantation at the Audie L. Murphy VA Hospital Bone Marrow Transplant Unit and at the University Hospital Bone Marrow Transplant Unit. We expect to enroll 400 patients during a 5-year period.

Methods: In order to answer the study questions, subjects will be assessed several times during the study period. The study involves a multidisciplinary group that will be evaluating and following the subjects. A baseline will be established by a physician and a nutritionist before the subjects start the high-dose chemotherapy regimen. The subjects will be followed with oral evaluations 3 times per week, beginning on the day of the transplant and ending when mucositis resolves, or the patient is discharged home, or 30 days post-transplant, whichever occurs first. At day 15 post-transplant, patients will be evaluated for the second time by the nutritionist. Further information such as blood values, use of medications and treatment complications, will be obtained by daily chart review.

Clinical relevance: Mucositis is, without a doubt, one of the most common and debilitating complications resulting from the intense cytotoxic therapies preceding hematopoietic stem cell transplantation. Mucositis is not only a problem for the patient who needs to deal with the pain and the rapidly decreasing quality of life, but it is also a problem for the health system. Mucositis frequently results in increased hospital length of stay, resulting in a significant increase in the cost of medical care. Multiple prophylactic and therapeutic attempts have been made in order to control the symptoms and the severity of mucositis. No prevention or cure is available for the disease. Despite the renewed interest in this complication, important gaps in knowledge remain in this area of the supportive care of cancer patients. These gaps in knowledge are wider in the area of mucositis in patients who undergo hematopoietic stem cell transplantation.

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Conditions studied

  • Peripheral Blood Stem Cell Transplantation

Keywords

  • Mucositis, hematopoietic stem cell transplantation, chemotherapy
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In context

Mucositis

488 studies on the registry are indexed under Mucositis; 70 are open to participants now.

This study's enrollment of 633 is above the median of 102 across 66 observational studies indexed under Mucositis.

Browse Mucositis studies →

Lead sponsor

The University of Texas Health Science Center at San Antonio is the lead sponsor of 435 studies on the registry; 88 are open to participants now.

Of its 62 completed or terminated interventional studies of FDA-regulated products, 31 (50%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients undergoing hematopoietic stem cell transplantation

Inclusion criteria

  • Patients undergoing hematopoietic stem cell transplantation
  • Age 18 years and older
  • Patients must understand and sign the study informed consent

Exclusion criteria

Exclusion Criteria:

  • None
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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
633 participants (actual)

Groups and cohorts

  • Obsevational

    Other: Mucositis and nutritional assessments

Interventions

  • OtherMucositis and nutritional assessments

    Mucositis and nutritional assessments before and during the hematopoietic stem cell transplantation

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What researchers measure

Primary outcomes

  1. To evaluate the incidence and severity of oral mucositis in patients undergoing high-dose chemotherapy and hematopoietic stem cell transplantation

    Time frame: 10 years

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Study locations

2 sites
  • Department of Veterans Affairs, South Texas Veterans Health Care System, Audie L. Murphy Memorial Veterans Hospital Division
    San Antonio, Texas 78229, United States
  • The University of Texas Health Science Center at San Antonio
    San Antonio, Texas 78229, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 21, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00575809
Lead sponsor
The University of Texas Health Science Center at San Antonio
Collaborators
South Texas Veterans Health Care System
Responsible party
Sponsor
First posted
Dec 18, 2007
Start date
May 2005
Primary completion
Jul 15, 2021
Completion
Jul 15, 2021
Last update
Jul 21, 2021

Study contacts

Cesar O Freytes, MD
principal investigator · South Texas Veterans Health Care System

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2021. You cannot join it, but the record below documents what was studied.

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