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Evaluation of combinational effect of Aprepitant on nausea and vomiting induced by chemotherapy (moderate risk) in patients with Gastric Cancer or Colorectal Cancer

Evaluation of combinational effect of Aprepitant on nausea and vomiting induced by chemotherapy (moderate risk) in patients with Gastric Cancer or Colorectal Cancer - Emend

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008041
Enrollment
100
Registered
2012-05-28
Start date
2012-02-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inoperable advanced/recurrence Gastric Cancer or Colorectal Cancer

Interventions

Group A: * 1st course : Conventional therapy (Palonosetron 0.75 mg i.v. on 1st day + Dexamathasone 9.9 mg i.v. on 1st day, 8 mg p.o. on 2nd day and 3rd day) * 2nd course : Conventional therapy (Palo

Sponsors

Osaka Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patient who has Gastric Cancer or Colorectal Cancer receiving FOLFILI, CPT-11 monotherapy, FOLFOX or XELOX regimen (2) Performance Status (ECOG)=0-2

Exclusion criteria

Exclusion criteria: (1) Patient who has severe liver failure or renal failure (2) Patient who has vomited or provoked nausea in the 24 hours prior to start of chemotherapy (3) Patient who has a factor that induces nausea or vomitting except chemotherapy (brain tumor, obstruction of gastrointestinal tract, active peptic ulcer, brain metastasis et al) (4) Patient who is considered inappropriate as a target patient by a physician-in-charge

Design outcomes

Primary

MeasureTime frame
* Frequency of vomiting * Severity of nausea

Secondary

MeasureTime frame
* Grading of appetite * Used amount of per-request medication

Countries

Japan

Contacts

Public ContactMasahiro Goto

Osaka Medical College Hospital Chemotherapy Cancter

in2030@poh.osaka-med.ac.jp072-683-1221

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026