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Clinical Trials/JPRN-UMIN000008552
JPRN-UMIN000008552
Completed
未知

A single-blind randomized controlled trial comparing Aprepitant plus (Granisetron)1st 5-HT3 receptor antagonist and Palonosetron for the prevention of chemotherapy-induced nausea and vomiting associated with moderately emetogenic chemotherapies including CBDCA in the gynecology cancer patients. - A single-blind randomized controlled trial for the prevention of chemotherapy-induced nausea and vomiting associated with moderately emetogenic chemotherapies in the gynecology cancer patients.

St. Mariannna University, School of Medicine0 sites300 target enrollmentAugust 1, 2012

Overview

Phase
未知
Intervention
Not specified
Conditions
Patients with gynecologic cancer receiving chemotherapy including carboplatin (that is, TC therapy: carboplatin + paclitaxel)
Sponsor
St. Mariannna University, School of Medicine
Enrollment
300
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 1, 2012
End Date
August 31, 2016
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\. Patients complicated with serious hepatic disorders or renal disorders. 2\. Patients with nausea and vomiting within 24 hours before initiation of cancer chemotherapy. 3\. Patients who used an antiemetic agent within 48 hours before initiation of cancer treatment. 4\. Patients with nausea and vomiting due to causes (brain tumor, digestive passage disorders, active peptic ulcer, brain metastasis, use of opioids, etc.) other than cancer chemotherapy. 5\. Patients with an associated disease, including uncontrolled diabetes, that prevents administration of dexamethasone for three days. 6\. Patients under medication with pimozide. 7\. Patients for whom abdominal radiotherapy is planned. 8\. Patients with a history of vomiting in past chemotherapy. 9\. Patients judged to be inappropriate for the study by the physician in charge.

Outcomes

Primary Outcomes

Not specified

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