NCT04726254

Brief Summary

The JuLi Registry seeks to fill some of the gaps associated with the clinical use of CBD (cannabidiol) and other cannabinoid formulations including THC and others. The overarching goal of this Registry is to rapidly advance research and understanding of the use of cannabis and hemp-based formulations, in the clinical community setting, when it is utilized to manage the symptoms of cancer treatment and other underlying health issues. These symptoms include nausea, neuropathy, and sleeplessness and chronic pain.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2021

Typical duration for all trials

Geographic Reach
1 country

4 active sites

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 24, 2021

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 27, 2021

Completed
6 months until next milestone

Study Start

First participant enrolled

August 1, 2021

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 15, 2024

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

February 15, 2025

Completed
Last Updated

July 19, 2022

Status Verified

July 1, 2022

Enrollment Period

2.5 years

First QC Date

January 24, 2021

Last Update Submit

July 15, 2022

Conditions

Outcome Measures

Primary Outcomes (2)

  • Symptom Relief

    Percentage of patients who obtain and report symptom relief, by symptom, condition and cannabis formulation

    3 months

  • Reduction in reliance on Rx medications

    Percentage of patients who report reduction or increase in use of Rx medications

    3 months

Secondary Outcomes (1)

  • Reduction in reliance on OTC medications

    3 months

Eligibility Criteria

Age21 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients greater than or equal to 21 years of age who are seeking to use hemp-based or cannabis-based formulations to relieve symptoms associated with medical interventions or conditions

You may qualify if:

  • years of age or older
  • Have requested from and/or decided with their providers to try CBD (hemp-based) or other cannabis products to relieve one or more symptoms related to a medical diagnosis
  • Consent to have their health data included in a Registry and participate in PRO (patient reported outcomes) surveys and data collection via a study app.

You may not qualify if:

  • Patient pregnant
  • Unwilling or unable to provide informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (4)

Precision Cancer Specialists

Los Gatos, California, 95032, United States

RECRUITING

Justin Lo MD

San Jose, California, 95128, United States

RECRUITING

Nashville Breast Center

Nashville, Tennessee, 37203, United States

RECRUITING

Dallas Surgical Group

Dallas, Texas, 75231, United States

RECRUITING

Related Publications (2)

  • Zou S, Kumar U. Cannabinoid Receptors and the Endocannabinoid System: Signaling and Function in the Central Nervous System. Int J Mol Sci. 2018 Mar 13;19(3):833. doi: 10.3390/ijms19030833.

    PMID: 29533978BACKGROUND
  • Freitas HR, Isaac AR, Malcher-Lopes R, Diaz BL, Trevenzoli IH, De Melo Reis RA. Polyunsaturated fatty acids and endocannabinoids in health and disease. Nutr Neurosci. 2018 Dec;21(10):695-714. doi: 10.1080/1028415X.2017.1347373. Epub 2017 Jul 7.

MeSH Terms

Conditions

Chronic PainFeeding and Eating DisordersAnxiety DisordersParasomniasNausea

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsSigns and Symptoms, DigestiveMental DisordersSleep Wake DisordersNervous System Diseases

Central Study Contacts

Mary Kay K Hardwick, MBA

CONTACT

Peter Beitsch, MD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
3 Months
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 24, 2021

First Posted

January 27, 2021

Study Start

August 1, 2021

Primary Completion

February 15, 2024

Study Completion

February 15, 2025

Last Updated

July 19, 2022

Record last verified: 2022-07

Locations