NCT00859495 · ADVERSE EVENTS
Adverse events
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
Adverse events occurred during the study; they are not necessarily caused by treatment. Serious events are not interchangeable with severe/grade 3–4 events. These safety populations may differ from efficacy populations.
- Collection time frame
- 20 weeks
- Other-event reporting threshold
- 5%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Multimodal Lung Sparing Regimen | 0 / 9 | 0 / 9 | 0 / 9 |
Serious adverse events
Other reported adverse events
Complete source fields
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 9
- description
- Intrapleural chemotherapy plus systemic chemotherapy: Thoracoscopy to implant two intrapleural catheters followed by intrapleural chemotherapy with doxorubicin and cisplatin (weeks 1, 2, 4, 5, 7, and 8). Systemic chemotherapy treatments with cisplatin and pemetrexed during weeks 3, 6, and 9. Intrapleural radiotherapy with P-32 will be given 3 weeks after last dose of chemotherapy and 11 to 12 weeks after initial thoracoscopy. Doxorubicin: A medication used in cancer chemotherapy, derived by chemical semisynthesis from a bacterial species. Cisplatin: Platinum-based antineoplastic Pemetrexed: Folate Analog Metabolic Inhibitor Radiotherapy: Standard procedure given 3 weeks after last dose of chemotherapy
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 9
- serious Num Affected
- 0
- serious Num At Risk
- 9
- title
- Multimodal Lung Sparing Regimen
- frequency Threshold
- 5
- time Frame
- 20 weeks
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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