Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING

Assessing Benefits and Harms of Cannabis/Cannabinoid Use Among Cancer Patients Treated in Community Oncology Clinics

NCT06418204 · View on ClinicalTrials.gov ↗

Study Summary

This is a multi-site clinical study enrolling 2000 newly diagnosed patients with breast, colorectal, melanoma, non-Hodgkin lymphoma, or non-small cell lung cancer, who are planning to receive one or more systemic cancer directed therapies with chemotherapy and/or (immune checkpoint inhibitors) ICIs.

Interventions

  • OTHER Non-interventional Study

Study Locations (20)

California

  • Kaiser Permanente-Deer Valley Medical Center — Antioch
  • Mission Hope Medical Oncology - Arroyo Grande — Arroyo Grande
  • PCR Oncology — Arroyo Grande
  • Mercy Cancer Center - Carmichael — Carmichael
  • Mercy San Juan Medical Center — Carmichael
  • Kaiser Permanente Dublin — Dublin
  • Mercy Cancer Center - Elk Grove — Elk Grove
  • Kaiser Permanente-Fremont — Fremont
  • Kaiser Permanente Fresno Orchard Plaza — Fresno
  • Kaiser Permanente-Fresno — Fresno
  • Saint Agnes Medical Center — Fresno
  • Saint Helena Hospital — Fresno
  • Contra Costa Regional Medical Center — Martinez
  • Contra Costa Regional Medical Center — Martinez
  • Kaiser Permanente- Modesto MOB II — Modesto

Arizona

  • Kingman Regional Medical Center — Kingman
  • Cancer Center at Saint Joseph's — Phoenix

Arkansas

  • Mercy Hospital Fort Smith — Fort Smith
  • NEA Baptist Memorial Hospital and Fowler Family Cancer Center - Jonesboro — Jonesboro

Alaska

  • Fairbanks Memorial Hospital — Fairbanks

Trial Details

FieldValue
Enrollment Target 2,000 participants
Start Date 2025-01-30
Est. Completion 2028-08-01

Sponsor

Wake Forest University Health Sciences

1,061 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06418204

The ClinicalTrials.gov registry entry for NCT06418204 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,061 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Melanoma appearing as the primary indexed condition, and to 1 intervention — of which Non-interventional Study is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06418204 reports 20 study locations spanning 4 distinct geographic areas — top geographies include California, Arizona, Arkansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06418204 about?

NCT06418204 is a clinical study titled "Assessing Benefits and Harms of Cannabis/Cannabinoid Use Among Cancer Patients Treated in Community Oncology Clinics". This is a multi-site clinical study enrolling 2000 newly diagnosed patients with breast, colorectal, melanoma, non-Hodgkin lymphoma, or non-small cell lung cancer, who are planning to receive one or more systemic cancer directed therapies with chemotherapy and/or (immune checkpoint inhibitors) ICIs.

What is the current status of trial NCT06418204?

This trial is currently recruiting. The enrollment target is 2,000 participants. The study started on 2025-01-30. Estimated completion is 2028-08-01.

What conditions does trial NCT06418204 study?

This clinical trial studies the following conditions: Melanoma, Breast Carcinoma, Non-Hodgkin Lymphoma, Colorectal Carcinoma, Lung Non-Small Cell Carcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06418204?

The interventions under investigation include: Non-interventional Study (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06418204?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,061 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06418204 being conducted?

This trial has 20 study locations across Alaska, Arizona, Arkansas, California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial