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Active Surveillance for Non-Small Cell Lung Cancer (ACTION-Lung Trial)
N/A
Waitlist Available
Research Sponsored by University of Vermont Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up two years
Awards & highlights
ACTION-Lung Trial Summary
This study is evaluating whether active surveillance is a good option for lung cancer patients.
Eligible Conditions
- Non-Small Cell Lung Cancer
- Lung Carcinoid Tumor
ACTION-Lung Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ one year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~one year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Primary Objective: Freedom-from radiation rate for patients on active surveillance
Secondary outcome measures
Secondary Objective: umber of participants on active surveillance with increased anxiety, depression, and uncertainty
Other outcome measures
Correlative Science Objective
Side effects data
From 2020 Phase 2 trial • 227 Patients • NCT027997459%
Hypertension
5%
Upper respiratory tract infection
4%
Fatigue
4%
Arthralgia
4%
Back pain
4%
Dysuria
4%
Pollakiuria
4%
Erectile dysfunction
3%
Gynaecomastia
2%
Weight decreased
1%
Angina pectoris
1%
Atrial fibrillation
1%
Cardiac tamponade
1%
Coronary artery perforation
1%
Abdominal pain
1%
Chronic sinusitis
1%
Basal cell carcinoma
1%
Bladder transitional cell carcinoma
1%
Malignant pleural effusion
1%
Haemorrhagic stroke
1%
Movement disorder
1%
Presyncope
1%
Pulmonary mass
1%
Physical disability
1%
Diarrhoea
1%
Nausea
1%
Libido decreased
1%
Breast tenderness
100%
80%
60%
40%
20%
0%
Study treatment Arm
Active Surveillance
Enzalutamide
ACTION-Lung Trial Design
1Treatment groups
Experimental Treatment
Group I: Active SurveillanceExperimental Treatment1 Intervention
Active surveillance is a way of either delaying or avoiding treatment and its possible side effects through carefully watching for changes in the tumor. Patients continue on this regimen, watching for tumor growth, up to 2 years on study or until rate or extent of growth leads to a shared decision to initiate treatment, whichever comes first.
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Who is running the clinical trial?
University of Vermont Medical CenterLead Sponsor
41 Previous Clinical Trials
25,799 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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