Nausea and vomiting. haematemesis (K92.0)haematemesisneonatal (P54.0)vomiting (of):excessive, in pregnancy (O21.-)following gastrointestinal surgery (K91.0)newborn (P92.0)psychogenic (F50.5)
Conditions
Interventions
Intervention 1: Intervention group:Patients received Zyntoma capsules 250 ml every 8 hours in a 3-day treatment period (Goldaru Pharmaceutical Co.). Intervention 2: Control group: Patients in the cont
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
6 Years to 18 Years
Inclusion criteria
Inclusion criteria: Patients undergoing chemotherapy Children over 6 years old
Exclusion criteria
Exclusion criteria: Heavy chemotherapy Discontinuation of chemotherapy for any reason
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome: treatment response which includes: presence/absence of chemotherapy-related nausea and vomiting. Timepoint: 3 days after treatment. Method of measurement: patient file; patient question. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome: patient's appetite after treatment. Timepoint: 3 days After treatment. Method of measurement: by Asking the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSamirarezayi
Tehran University of Medical Sciences
Outcome results
None listed