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A multicenter real-world clinical study on the compliance of ondansetron hydrochloride tablets in the treatment of chemotherapy-induced nausea and vomiting during the entire course of medication and the comparison of the efficacy of changing/stopping medication midway

A multicenter real-world clinical study on the compliance of ondansetron hydrochloride tablets in the treatment of chemotherapy-induced nausea and vomiting during the entire course of medication and the comparison of the efficacy of changing/stopping medication midway

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087061
Enrollment
Unknown
Registered
2024-07-18
Start date
2024-07-22
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Chemotherapy induced nausea and vomiting

Interventions

Case series:None

Sponsors

Beijing Chaoyang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age = 18 years old; 2. Diagnosed as malignant tumor by pathological histology or cytology, regardless of tumor type TNM staging and previous chemotherapy status; 3. Researchers believe that chemotherapy induced nausea and vomiting should be prevented or treated with antiemetic drugs

Exclusion criteria

Exclusion criteria: 1. Individuals who have experienced symptoms such as nausea and vomiting one week prior to enrollment; 2. For 5-HT3 receptor antagonists, dexamethasone NK-1 receptor antagonists, allergic reactions to olanzapine; 3. Patients taking opioid drugs; 4. Suffering from central nervous system disorders or mental system disorders; 5. Patients with active infections or severe complications; 6. Pregnant or lactating population; 7. Other situations deemed unsuitable by researchers, such as active pulmonary tuberculosis and severe coagulation dysfunction

Design outcomes

Primary

MeasureTime frame
The proportion of subjects who complete remission within 7 days after the end of each cycle of chemotherapy treatment;

Secondary

MeasureTime frame
Compliance of oral ondansetron hydrochloride tablets measured at each chemotherapy cycle;The reasons affecting the compliance of ondansetron hydrochloride tablets;After each cycle of chemotherapy, the subjects will receive a QOL questionnaire for quality of life scores;Adverse events during the treatment of 5-HT3 receptor antagonists;

Countries

China

Contacts

Public ContactWenming CHEN

Beijing Chaoyang Hospital, Capital Medical University

13910107759@163.com+86 10 8523 1043

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026