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NCT02611037 · ClinicalTrials.gov registry record · Phase 2
Transarterial Chemoperfusion: Cisplatin, Methotrexate, Gemcitabine for Unresectable Pleural Mesothelioma
A Phase 2 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.
- Completed
- Registry status
- Phase 2
- Development phase
- 34
- Enrollment target
NCT02611037 is a Phase 2 study that has completed, run by H. Lee Moffitt Cancer Center and Research Institute. The registered enrollment target is 34 participants.
The verdict
NCT02611037, a Phase 2 study, has completed, sponsored by H. Lee Moffitt Cancer Center and Research Institute.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 34 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether the transarterial chemoperfusion treatment with cisplatin, methotrexate and gemcitabine is safe and effective in adults with malignant pleural mesothelioma (MPM).
Interventions
- DRUG Cisplatin
- DRUG Gemcitabine
- DRUG Methotrexate
- OTHER Lung Cancer Symptom Scale for Mesothelioma Questionnaire
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 34 participants |
| Start Date | 2016-03-04 |
| Est. Completion | 2024-01-26 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02611037
The ClinicalTrials.gov registry entry for NCT02611037 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 34 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is H. Lee Moffitt Cancer Center and Research Institute, which has 502 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which Cisplatin is the first listed.
NCT02611037 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02611037 about?
NCT02611037 is a clinical study titled "Transarterial Chemoperfusion: Cisplatin, Methotrexate, Gemcitabine for Unresectable Pleural Mesothelioma". The purpose of this study is to determine whether the transarterial chemoperfusion treatment with cisplatin, methotrexate and gemcitabine is safe and effective in adults with malignant pleural mesothelioma (MPM).
What is the current status of trial NCT02611037?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 34 participants. The study started on 2016-03-04. Estimated completion is 2024-01-26.
What interventions are being tested in trial NCT02611037?
The interventions under investigation include: Cisplatin (DRUG), Gemcitabine (DRUG), Methotrexate (DRUG), Lung Cancer Symptom Scale for Mesothelioma Questionnaire (OTHER).
Who is sponsoring clinical trial NCT02611037?
This trial is sponsored by H. Lee Moffitt Cancer Center and Research Institute, which has 502 total clinical trials registered on ClinicalTrials.gov.
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