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Clinical Trial Summary

This study evaluates the possibility to reduce the total dose of dexamethasone, when administered with NEPA, to prevent chemotherapy-induced nausea and vomiting (CINV) in Non-Small Cell Lung Cancer (NSCLC) patients receiving a cisplatin-based chemotherapy


Clinical Trial Description

On day 1 (day of chemotherapy), all eligible patients will receive oral NEPA (300 mg netupitant/0.5 mg palonosetron), 60 minutes before chemotherapy, and intravenous dexamethasone 12 mg, 30 minutes before chemotherapy initiation.

For the prevention of delayed CINV, patients will be assigned randomly to one of the following treatment arms:

- Test arm A: no further anti-emetic prophylaxis on days 2 thorough 4;

- Test arm B: oral dexamethasone 4 mg once per day in the morning of days 2 and 3;

- Reference arm C: oral dexamethasone 4 mg twice per day on days 2 thorough 4. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04201769
Study type Interventional
Source Consorzio Oncotech
Contact
Status Active, not recruiting
Phase Phase 3
Start date November 25, 2016
Completion date April 2020

See also
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