Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03909620
Other study ID # NK/5292/DM/760
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2019
Est. completion date December 31, 2021

Study information

Verified date March 2022
Source Postgraduate Institute of Medical Education and Research
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Lung cancer screening with low-dose computed tomography (LDCT) has been recently shown to result in a significant reduction in lung cancer-specific mortality. However, the utility of LDCT screening in developing countries with high incidence of tuberculosis has not been adequately studied. The investigators hypothesize that LDCT screening in tuberculosis endemic regions is likely to yield a large proportion of false-positive results, especially in the initial round of screening, posing a significant burden on the healthcare system. Herein, the investigators assess the utility of LDCT and its cost-effectiveness in India.


Description:

Screening for lung cancer may reduce lung cancer mortality by diagnosing the disease at an early stage when it is treatable more effectively. There are several methods available for screening of lung cancer. These include sputum cytology, chest radiography, computed tomography (CT) of the chest, and positron emission tomography (PET). However, sputum cytology and chest radiography have been found to be ineffective as screening tests for lung cancer as there is no reduction in lung cancer mortality. The use of CT or PET for lung cancer screening may be associated with unacceptable levels of radiation exposure and enormous cost. Low-dose computed tomography (LDCT) of the chest is a special type of CT, which uses relatively low radiation exposure to create a low-resolution image of the entire thorax. The radiation exposure associated with LDCT is 5-6 times less than that of a conventional CT scan of the thorax. LDCT screening has been to shown to result in a 20% reduction in lung cancer-specific mortality. Several national and international guidelines recommend this strategy for lung cancer screening. Despite these guidelines and recommendations by several organizations, lung cancer screening has not been established in several developing countries, where a controversy arises due to high rates of granulomatous diseases like tuberculosis. Emerging evidence indicates that false positive results with LDCT in developing countries may not be unacceptably high as previously believed. In this study, the investigators intend to assess the utility of lung cancer screening using low-dose computed tomography (LDCT) in India, a country with high prevalence of tuberculosis.


Recruitment information / eligibility

Status Completed
Enrollment 253
Est. completion date December 31, 2021
Est. primary completion date March 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 74 Years
Eligibility Inclusion Criteria: - Individuals aged 55-74 years with at least 30 pack-year history of smoking (or smoking index =600) who are current smokers or quit within the last 15 years OR - Individuals aged 50-74 years with at least 20 pack-year history of smoking (or smoking index =400) who are current or former smokers with COPD or family history of lung cancer in any first-degree relative Exclusion Criteria: - Symptomatic structural lung disease other than COPD (e.g. bronchiectasis, chronic pulmonary aspergillosis, pulmonary fibrosis) - Severe comorbid condition which is likely to limit the survival of the patient in the opinion of the investigator (e.g. advanced lung disease, cardiovascular disease, chronic kidney disease, chronic liver disease) - Presence of symptoms which lead to a suspicion of lung cancer (e.g. hemoptysis or unexplained weight loss [>5 kg] within the last 6 months) - Conditions which may interfere interpretation of CT (e.g. metallic implants on chest wall, cardiac pacemakers) - Treatment for any other cancer in the last 5 years - Pulmonary infection (for which treatment with antimicrobials is indicated) which is active at present or was recent (within the last 3 months) - Patients who have underwent CT chest within the last 18 months - Negative consent

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Low-dose computed tomography of chest
Eligible subjects will undergo a single round of LDCT screening. The LDCT will be considered as positive if a solid nodule or part-solid nodule of size =6 mm or non-solid nodule of size =20 mm is identified. Evaluation of positive nodules will be performed as per existing standard recommendations

Locations

Country Name City State
India Postgraduate Institute of Medical Education and Research (PGIMER) Chandigarh

Sponsors (1)

Lead Sponsor Collaborator
Postgraduate Institute of Medical Education and Research

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Positivity rate with LDCT screening The proportion of participants with a positive result among the total number of individuals screened with LDCT After baseline LDCT scan results are available (an average of 1 week after LDCT scan)
Secondary Rate of detection of lung cancer Rate of lung cancer detection among study participants Up to 6 months after the LDCT scan
Secondary False positive rate Rate of false positive results with LDCT screening Up to 6 months after the LDCT scan
Secondary Proportion of patients requiring additional procedures (imaging/invasive procedures) The proportion of patients with positive results on initial LDCT scan requiring additional procedures (imaging/invasive procedures) Up to 6 months after the LDCT scan
Secondary Proportion of patients developing complications due to additional procedures The proportion of patients among those who developed complications due to additional procedures (imaging/invasive procedures) performed after initial LDCT scan Up to 2 weeks after the diagnostic procedure
Secondary Change in the 6-item Spielberger State-Trait Anxiety Inventory (STAI-6) questionnaire score Change in anxiety levels from baseline after conveying LDCT results to the patient After communication of baseline LDCT results (an average of 1-2 weeks after the LDCT scan)
Secondary Cost in Indian Rupees to detect one case of lung cancer by LDCT screening Cost-effectiveness of LDCT screening Up to 6 months after the LDCT scan
Secondary Proportion of patients who quit/re-initiated smoking after inclusion in study The proportion of patients who quit/re-initiated smoking after inclusion in study Up to 6 months after the LDCT scan
See also
  Status Clinical Trial Phase
Completed NCT03918538 - A Series of Study in Testing Efficacy of Pulmonary Rehabilitation Interventions in Lung Cancer Survivors N/A
Recruiting NCT05078918 - Comprehensive Care Program for Their Return to Normal Life Among Lung Cancer Survivors N/A
Active, not recruiting NCT04548830 - Safety of Lung Cryobiopsy in People With Cancer Phase 2
Completed NCT04633850 - Implementation of Adjuvants in Intercostal Nerve Blockades for Thoracoscopic Surgery in Pulmonary Cancer Patients
Recruiting NCT06037954 - A Study of Mental Health Care in People With Cancer N/A
Recruiting NCT06006390 - CEA Targeting Chimeric Antigen Receptor T Lymphocytes (CAR-T) in the Treatment of CEA Positive Advanced Solid Tumors Phase 1/Phase 2
Recruiting NCT05583916 - Same Day Discharge for Video-Assisted Thoracoscopic Surgery (VATS) Lung Surgery N/A
Completed NCT00341939 - Retrospective Analysis of a Drug-Metabolizing Genotype in Cancer Patients and Correlation With Pharmacokinetic and Pharmacodynamics Data
Not yet recruiting NCT06376253 - A Phase I Study of [177Lu]Lu-EVS459 in Patients With Ovarian and Lung Cancers Phase 1
Recruiting NCT05898594 - Lung Cancer Screening in High-risk Black Women N/A
Active, not recruiting NCT05060432 - Study of EOS-448 With Standard of Care and/or Investigational Therapies in Participants With Advanced Solid Tumors Phase 1/Phase 2
Active, not recruiting NCT03667716 - COM701 (an Inhibitor of PVRIG) in Subjects With Advanced Solid Tumors. Phase 1
Active, not recruiting NCT03575793 - A Phase I/II Study of Nivolumab, Ipilimumab and Plinabulin in Patients With Recurrent Small Cell Lung Cancer Phase 1/Phase 2
Terminated NCT01624090 - Mithramycin for Lung, Esophagus, and Other Chest Cancers Phase 2
Terminated NCT03275688 - NanoSpectrometer Biomarker Discovery and Confirmation Study
Not yet recruiting NCT04931420 - Study Comparing Standard of Care Chemotherapy With/ Without Sequential Cytoreductive Surgery for Patients With Metastatic Foregut Cancer and Undetectable Circulating Tumor-Deoxyribose Nucleic Acid Levels Phase 2
Recruiting NCT06010862 - Clinical Study of CEA-targeted CAR-T Therapy for CEA-positive Advanced/Metastatic Malignant Solid Tumors Phase 1
Recruiting NCT06052449 - Assessing Social Determinants of Health to Increase Cancer Screening N/A
Not yet recruiting NCT06017271 - Predictive Value of Epicardial Adipose Tissue for Pulmonary Embolism and Death in Patients With Lung Cancer
Recruiting NCT05787522 - Efficacy and Safety of AI-assisted Radiotherapy Contouring Software for Thoracic Organs at Risk