Status:
UNKNOWN
Olanzapine Combined With Fosaprepitant, Ondansetron, and Dexamethasone for Preventing Nausea and Vomiting in Patients With Testicular Cancer
Lead Sponsor:
Shi Yanxia
Conditions:
Olanzapine
CINV
Eligibility:
MALE
16+ years
Phase:
PHASE3
Brief Summary
This study aims to investigate the efficacy and safety of olanzapine combined with fosaprepitant, ondansetron and dexamethasone compared with placebo combined with fosaprepitant, ondansetron and dexam...
Detailed Description
This is a prospective, randomized, double-blind, placebo-controlled, cross-over Phase III clinical study. A total of 75 patients were enrolled in two sequential treatment groups (olanzapine-placebo a...
Eligibility Criteria
Inclusion
- Inclusion Criteria
- Patients must meet the following criteria for inclusion:
- Pathology confirmed germ cell tumor (both spermatogonoma and non-spermatogonoma) and had no chemotherapy before;
- Men;
- Age ≥16 years old;
- ECOG score of physical status 0-2;
- Chemotherapy regimen containing 5-day cisplatin (20mg/m2, 100mg total;
- No other nausea, vomiting, or use of any antiemetics within 72 hours prior to enrollment;
- There are no clear brain metastases or other reasons for long-term systemic use of hormones;
- The general condition is good, and the blood, liver and kidney functions meet the following standards:
- Hemoglobin: 90 g/L and above White blood cell count: 3.5 \* 109 / L - 10.0 \*109 / L Neutrophil count: 1.5\* 109/L or above Platelet count: 90\* 109/L or above Serum total bilirubin: below 1.5 times the upper limit of normal Serum AST, ALT and ALP: the upper limit of normal is below 2.5 times when the patient is present
- Ability to read, understand and complete research questionnaires and journals, including visual analog scale (VAS);
- Understand the study procedure and sign the informed consent in person to participate in the study
- Exclusion Criteria
- Patients who meet any of the following criteria will be excluded:
- Digestive tract obstruction, water and electrolyte disorder;
- Have central nervous system diseases (such as primary brain tumors, uncontrolled seizures, any history of brain metastases or strokes);
- Contraindications to the use of glucocorticoids: ① Viral, bacterial, fungal and other infections that cannot be controlled by antibiotics;② Active gastric or duodenal ulcer;③ Severe hypertension, arteriosclerosis, diabetes; ④ Osteoporosis;⑤ Corneal ulcer;⑥Trauma or surgical repair period, fracture; ⑦Adeno-cortical hyperfunction; ⑧Severe mental illness and epilepsy; ⑨ patients with cardiac or renal dysfunction;
- Patients with mental disabilities or severe emotional or mental disorders are considered unsuitable for inclusion in the study;
- In addition to malignancy, the patient has an active infection (e.g. pneumonia, hepatitis) or any uncontrolled infection diseases (such as diabetic ketoacidosis), and the researchers believe may contribute to the study's findings confounding, or exposing patients receiving study drugs to unnecessary risks;
- The patient is currently using any prohibited drugs, including medicinal marijuana or is currently using alcohol (Chinese Diagnostic criteria for drug dependence);
- The patient received an unapproved (experimental) drug treatment within the past 4 weeks;
- Taking oral olanzapine or other psychotropic drugs;
- A history of hypersensitivity to fosappitan, 5-HT3 receptor antagonists or dexamethasone;
- The patient cannot swallow the drugs;
- The principal investigator considered the patients unsuitable for the study;
- Inability or unwillingness to adhere to research protocols
Exclusion
Key Trial Info
Start Date :
January 18 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 31 2024
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT05244577
Start Date
January 18 2022
End Date
March 31 2024
Last Update
February 6 2023
Active Locations (1)
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1
Sun Yat-sen University
Guangzhou, Guangdong, China, 510060