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Treatment of Chemotherapy-induced Nausea and Vomiting

Phase 2
Completed
Conditions
Nausea
Vomiting
Interventions
Registration Number
NCT01101529
Lead Sponsor
Uppsala University Hospital
Brief Summary

Delayed nausea is a common problem after high dose chemotherapy for bone marrow transplantation. This study wants to compare standard prophylactic anti-emetic therapy with the same treatment plus the drug aprepitant (Emend). The hypothesis is that addition of Emend will reduce nausea and vomiting.

Detailed Description

A single centre randomized placebo-controlled phase II-study with a random assignment to experimental (EXP) or control (CTR) group. All patients with lymphoproliferative diseases ≥18 years of age, scheduled for myeloablative therapy before autologous stem cell transplantation at the Akademiska University Hospital in Uppsala, Sweden, will be included consecutively during one and a half year. A total of 90 patients (45 per treatment arm) will be accrued for this study. They will be invited by mail to participate in the study a couple of weeks before hospital entry. A random assignment to EXP or CTR will be performed by research nurses not participating in any other way in the study. Patients will be stratified for diagnosis which also means myeloablative therapy (lymphoma (BEAC) or myeloma (high-dose melphalan)), and the groups are expected to be similar in size. One box for each diagnosis (lymphoma and myeloma) will contain equal numbers of randomisation cards for the experimental and control groups, randomly mixed within each box. Cards will be picked consecutively by a research nurse not otherwise involved in the study. The EXP group will receive aprepitant (EMEND®) in combination with standard anti-emetic treatment and the CTR group will receive standard anti-emetic treatment. All treatment will be given in the hospital.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
90
Inclusion Criteria
  • Age ≥18 years
  • Able to communicate in Swedish
  • Diagnosis of lymphoproliferative disease
  • Scheduled for myeloablative therapy and autologous stem cell transplantation
  • Written informed consent
  • Able to swallow oral medications
Exclusion Criteria
  • Nausea at baseline (immediately before start of chemotherapy)
  • Gastrointestinal obstruction or active peptic ulcer
  • Current illness requiring chronic systemic steroids or requirement for chronic use of antiemetic agent(s)
  • Hypersensitivity to any component of the study regimen
  • Pregnancy or nursing
  • Unrelenting hiccups
  • Radiation therapy to pelvis or abdomen within 1 week before or after study day 1
  • Psychiatric illness or multi-system organ failure
  • Hepatic insufficiency with ASAT, ALAT three times over reference value
  • Renal insufficiency with creatinin value three times over reference value.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Standard antiemetic therapy plus placeboPlaceboStandard anti-emetic prophylaxis consisting of 1/dexamethasone 6 mg daily during the chemotherapy days and 2/tropisetron (Navoban)5 mg daily during chemotherapy and 2 days after
aprepitant (Emend)Aprepitant (Emend)Aprepitant given orally 125 mg the first day, then 80 mg daily during the chemotherapy course and 7 days after as an addition to standard antiemetic therapy as in the placebo arm.
Primary Outcome Measures
NameTimeMethod
Vomiting and nausea7 days

The proportion of patients with a complete response (no vomiting and/or only mild nausea and no use of rescue therapy) a/ during chemotherapy and b/ in the delayed phase (up to 7 days after end of chemotherapy).

Secondary Outcome Measures
NameTimeMethod
Safety and tolerability of the aprepitant regimen for CINV3 weeks

Possible side effects will be recorded, and all AE:s reported during 3 weeks after the chemotherapy.

Trial Locations

Locations (1)

Uppsala University Hospital

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Uppsala, Sweden

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