Efficacy and Safety of Argon Plasma Coagulation in the Treatment of Patients With Hemoptysis Caus… (NCT03625947) | Clinical Trial Compass
TerminatedNot Applicable
Efficacy and Safety of Argon Plasma Coagulation in the Treatment of Patients With Hemoptysis Caused by Endobronchial Malignancies
Stopped: Recruitment issues during pandemic (2020-2021)
Italy75 participantsStarted 2018-08-08
Plain-language summary
The aim of this study is to evaluate the efficacy, the safety and the main predictors of success of bronchoscopic Argon Plasma Coagulation in patients with hemoptysis caused by endobronchial malignancies.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Adult patients with hemoptysis caused by endobronchial (i.e. identifiable with flexible bronchoscopy) malignancies, without coagulopathy or other medically correctable causes of bleeding, who need endoscopic intervention with Argon Plasma Coagulation to stop bleeding
* Adult patients who are able to tolerate bronchoscopy
* Adult patients who are able to sign the written informed consent for the study participation
Exclusion Criteria:
* Patients with hemoptysis caused by endobronchial malignancies with coagulopathy or other medically correctable causes of bleeding.
* Patients who are not able to tolerate bronchoscopy
* Patients with hemoptysis without identifiable endobronchial malignancies during flexible bronchoscopy
* Patients with Pace-Maker and/or Automated Implantable Cardioverter- Defibrillator(AICD)
* Patients who refuse/are not able to sign the informed consent for the study participation
What they're measuring
1
Percentage of patients with bleeding cessation without recurrence at 48 after bronchoscopic Argon Plasma Coagulation