Determining Clinical Study Experiences of Chronic Lymphocytic Leukemia Patients
NCT ID: NCT05899543
Last Updated: 2023-06-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
500 participants
OBSERVATIONAL
2024-07-31
2026-07-31
Brief Summary
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This trial will scrutinize the experiences of patients diagnosed with chronic lymphocytic leukemia as they take part in a separate medical intervention clinical trial. The focus will be on tracking the rates of completion and withdrawal among these individuals.
It will also try to analyze data from the perspective of different demographic groups to check for recurring trends which might yield insights for the sake of future chronic lymphocytic leukemia patients.
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Detailed Description
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Conditions
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Study Design
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CASE_CROSSOVER
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patient is a minimum of 18 years or older
* Able to comprehend the investigational nature of the protocol and provide informed consent
Exclusion Criteria
* Patients who are currently receiving any other investigational drug
* Any mental or medical condition that prevents the patient from giving informed consent or participating in the trial
18 Years
ALL
No
Sponsors
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Power Life Sciences Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Michael B Gill
Role: STUDY_DIRECTOR
Power Life Sciences Inc.
Locations
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Power Life Sciences
San Francisco, California, United States
Countries
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Central Contacts
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References
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Nabhan C, Rosen ST. Chronic lymphocytic leukemia: a clinical review. JAMA. 2014 Dec 3;312(21):2265-76. doi: 10.1001/jama.2014.14553.
Iskierka-Jazdzewska E, Robak T. Investigational treatments for chronic lymphocytic leukemia: a focus on phase 1 and 2 clinical trials. Expert Opin Investig Drugs. 2020 Jul;29(7):709-722. doi: 10.1080/13543784.2020.1770225. Epub 2020 May 27.
Molica S. The clinical safety of ibrutinib in chronic lymphocytic leukemia. Expert Opin Drug Saf. 2015 Oct;14(10):1621-9. doi: 10.1517/14740338.2015.1084286. Epub 2015 Sep 11.
Provided Documents
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Document Type: Informed Consent Form
Other Identifiers
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83115421
Identifier Type: -
Identifier Source: org_study_id
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