Clinical trials

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Condition / disease
Location
Status: Recruiting

Dolasetron for the Prevention of CINV in Children With Acute Lymphoblastic Leukemia

This is a prospective, multicenter, real-world study of 500 participants with childhood acute lymphoblastic leukemia who are scheduled to receive dolasetron mesylate injection for prophylaxis against chemotherapy-induced nausea and vomiting. This study did not make any decision or process intervention for clinical antitumor therapy. The study plans to observe the control of nausea and vomiting within 120 h (D1-D5) after receiving induction chemotherapy and the safety within 7 days (or until this discharge, whichever occurs first). During the whole study, demographic data, history of motion sickness, ECOG score, complications, name and dosage of anti-tumor therapy drugs, this antiemetic regimen, nausea and vomiting, rescue therapy drugs, combined drugs and adverse events were recorded.

Participants needed: 500
Trial details
Age: 2-17Biological sex: AllType: ObservationalSponsor: Anhui Provincial Children's HospitalUpdated: Jan 1, 2025Locations: 1Duration: 1 Week
Eligibility criteria

Age 2~17 years old [+5]

Allergic to Dolasetron mesylate injection and its excipients [+2]