Examining Clinical Trial Participation for Small Cell Lung Cancer Patients
Studying Patient Experiences in Small Cell Lung Cancer Clinical Trials to Identify Influencing Factors
1 other identifier
observational
500
0 countries
N/A
Brief Summary
Clinical study participation percentages haven't always been fully representative of a given demographic. The goal is to find out which aspects of a clinical trial may make it more difficult for patients to take part or see it through. The data will be evaluated through different demographic lenses and identify trends that could help improve the experience of future small cell lung cancer patients during clinical trials.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2024
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 2, 2023
CompletedFirst Posted
Study publicly available on registry
March 15, 2023
CompletedStudy Start
First participant enrolled
April 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2026
CompletedApril 3, 2023
March 1, 2023
1 year
March 2, 2023
March 31, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Rate of patients who decide to enroll in a small cell lung cancer clinical study.
3 months
Number of small cell lung cancer patients who remain in clinical trial until completion.
12 months
Eligibility Criteria
Small cell lung cancer patients who are actively considering involvement in an observational clinical trial, but have not yet completed enrollment and registration.
You may qualify if:
- Aged ≥ 18 years old and ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed.
- Participant has a diagnosis of small cell lung cancer.
- Willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.
You may not qualify if:
- Patients with any significant history of non-compliance to medical regimens or with inability to grant a reliable informed consent.
- Pregnant or lactating woman
- Known medical condition that, in the investigator's opinion, would increase the risk associated with study participation or study drug(s) administration or interfere with the interpretation of safety results
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (3)
van Meerbeeck JP, Fennell DA, De Ruysscher DK. Small-cell lung cancer. Lancet. 2011 Nov 12;378(9804):1741-55. doi: 10.1016/S0140-6736(11)60165-7. Epub 2011 May 10.
PMID: 21565397BACKGROUNDSeto Z, Takata N, Murayama N, Tokui K, Okazawa S, Kambara K, Imanishi S, Miwa T, Hayashi R, Matsui S, Inomata M. Irinotecan monotherapy as third- or further-line treatment for patients with small cell lung cancer. Tumori. 2021 Dec;107(6):536-541. doi: 10.1177/0300891620974762. Epub 2020 Nov 25.
PMID: 34847814BACKGROUNDXing H, Zhang J, Ge F, Yu X, Bian H, Zhang F, Fang J. [Analysis of the Efficacy of Irinotecan in the Second-line Treatment of Refractory and Relapsed Small Cell Lung Cancer]. Zhongguo Fei Ai Za Zhi. 2021 Mar 20;24(3):167-172. doi: 10.3779/j.issn.1009-3419.2021.103.04. Chinese.
PMID: 33819966BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Michael B Gill
Power Life Sciences Inc.
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CROSSOVER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 2, 2023
First Posted
March 15, 2023
Study Start
April 1, 2024
Primary Completion
April 1, 2025
Study Completion
April 1, 2026
Last Updated
April 3, 2023
Record last verified: 2023-03