The First Affiliated Hospital of Guangzhou Medical University
Guangzhou, China
NCT Number: NCT03448146
This trial was to evaluate the efficacy of intratumoral PTS injection in alleviating airway obstruction and dyspnea by improving the percentage of lumen patency of patients with central air way NSCLC tumor severe obstruction.
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Notify Me18 year–83 year
All sexes
Interventional
Phase 3
Guangzhou, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: PTS
Time frame: 30 days after the last treatment
The objective response rate of target lesions in patients with central air way NSCLC tumor severe obstruction after PTS treatment were evaluated based on measurement results of CT and bronchoscopy.
Time frame: 30 days after the last treatment
The improvement rate of luminal obstructions in patients with central air way NSCLC tumor severe obstruction after PTS treatment were evaluated based on measurement results of CT and bronchoscopy.
Time frame: 30 days after the last treatment
Changes in Forced Vital Capacity (FVC)
Time frame: 30 days after the last treatment
Changes in Forced Expiratory Volume in One Second (FEV1)/Forced Vital Capacity (FVC)
Time frame: 30 days after the last treatment
Changes in Baseline Dyspnea Index (BDI) score. The BDI provides a multidimensional measurement of dyspnea based on 3 domains: functional impairment, magnitude of task and magnitude of effort that evoke dyspnea in activities of daily living, in symptomatic individuals. Rated in five grades from 0 to 4 for each domain. Ranging from 0 to 12. The lower the score, the worse the severity of dyspnea.
Time frame: 30 days after the last treatment
Changes in pleural effusion
Time frame: 30 days after the last treatment
Changes in Eastern Cooperative Oncology Group (ECOG) performance status
Time frame: 30 days after the last treatment
Changes in Quality of Life (QOL) score. Quality of life (QOL) was evaluated based on the subject's answers in Functional Assessment of Cancer Therapy-Lung Cancer Subscale (FACT-LCS) questionnaire, version 4. Symptoms of lung cancer were evaluated according to the completed Lung Cancer Subscale (LCS). The FACT-LCS, version 4 is a patient completed questionnaire consisting 36 items that assesses health related quality of life (HRQL) in lung cancer patients. The FACT-LCS, version 4 consists of the 27-item FACT-G assessing generic HRQL concerns and 9-item Lung Cancer Subscale assessing disease-specific issues. Instrument scoring yields a range from 0 to 144 with higher scores representing better patient status.
Time frame: 30 days after the last treatment
Duration of response (DOR) of target lesion
PTS International Inc.
Industry
A Phase III Single Arm Trial of PTS (Para Toluenesulfonamide Injection) Via Bronchoscopy Intervention Intratumoral Injection in Patients With Central Air Way NSCLC Tumor Severe Obstruction
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