TerminatedPhase 4NCT04155008

Nutrition and Pharmacological Algorithm for Oncology Patients Study

Loss of appetite is a common symptom of patients with cancer and can cause distress which impacts patients and caregivers. Patients diagnosed with head/neck, lung or pancreatic cancer will be recruited for this study to decrease the suffering and distress associated with eating during cancer treatment and improve the quality of life of patients by implementing an algorithm utilizing nutrition intervention and appetite stimulants.

Checked against the public recordLast updated Nov 16, 2022 · Source: ClinicalTrials.gov

StatusTerminated
PhasePhase 4
U.S. locations1
SponsorMontefiore Medical Center
01
Study overview

What this study is about

Purpose
Supportive Care
Study type
Interventional
Phase
Phase 4
Sponsor
Montefiore Medical Center
Interventions being studied
Drug: Dexamethasone; Drug: Dronabinol; Drug: Mirtazapine; Behavioral: Nutrition Intervention
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: 1. Patients with a diagnosis of head/neck, lung, pancreatic cancer, or metastatic cancer from any solid tumor 2. Planned, ongoing, or recently treated patient (within the past 30 days) with chemotherapy, immunotherapy, and/or intravenous targeted biologic therapy 3. No previous use of appetite stimulants 4. All patients must sign study specific informed consent prior to being included in the study 5. No contraindication to appetite stimulants Exclusion Criteria: 1. Patient \<18 years old 2. Contraindication to appetite stimulants

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Montefiore HospitalThe Bronx, New York

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Nov 16, 2022. Always confirm current availability with the study team.

View original record ↗