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PARP Inhibitors-induced nausea and vomiting in patients with gynecologic cancer: a prospective, observational, multicenter study.

Not Applicable
Conditions
Ovarian cancer
Registration Number
JPRN-UMIN000039076
Lead Sponsor
Gifu University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
Female
Target Recruitment
234
Inclusion Criteria

Not provided

Exclusion Criteria

1.Patients with a reduction in the initial dose of olaparib and niraparib 2.Patients who need antiemetics at the enrollment. 3.Patients who start taking opioids within 48 hours prior to enrollment 4.Patients with ascites effusion requiring paracentesis 5.Patients with symptomatic brain metastases and cancerous meningitis 6.Patients who have gastrointestinal obstruction 7.Patients who received abdominal or pelvic irradiation within 6 days prior to enrollment 8.Patients who use any drug with antiemetic activity, including NK1RA, 5-HT3RA, corticosteroids, dopamine receptor antagonists, phenothiazine tranquilizers, SSRI, SNRI, SDA, MARTA within 6 days prior to enrollment 9.Other patients who are judged to be inappropriate for the study by the investigator

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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