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Genotyping Intervention Supportive Care for Chemotherapy

N/A
Waitlist Available
Led By Rhonda Cooper-DeHoff, Pharm D, MS
Research Sponsored by University of Florida
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at pre-chemotherapy (baseline), 2 weeks, 4 weeks, and 12 weeks post initiation of chemotherapy.
Awards & highlights

Summary

This trial tests if using genetic information to guide medication choices can improve the well-being of cancer patients undergoing chemotherapy. It aims to find out if this approach reduces symptoms and side effects compared to usual care.

Eligible Conditions
  • Chemotherapy
  • Supportive Care
  • Genotyping

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at pre-chemotherapy (baseline), 2 weeks, 4 weeks, and 12 weeks post initiation of chemotherapy.
This trial's timeline: 3 weeks for screening, Varies for treatment, and at pre-chemotherapy (baseline), 2 weeks, 4 weeks, and 12 weeks post initiation of chemotherapy. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in patient MDASI scoring
Secondary outcome measures
Pharmaceutical Preparations

Trial Design

2Treatment groups
Active Control
Group I: Genotyping Intervention Supportive CareActive Control1 Intervention
For those randomized to the genotype intervention group, genotype results will be returned in the EHR pre-emptively and supportive care will be prescribed based on genotype results.
Group II: Delayed Genotyping Intervention Supportive CareActive Control1 Intervention
For those randomized to the delayed genotype intervention group, supportive care will be prescribed based on usual clinical practice.

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Who is running the clinical trial?

University of FloridaLead Sponsor
1,354 Previous Clinical Trials
713,198 Total Patients Enrolled
Rhonda Cooper-DeHoff, Pharm D, MSPrincipal InvestigatorUniversity of Florida
~24 spots leftby Sep 2025
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