A Study to Assess the Anti-Emetic Efficacy of Ginger in Children and Adolescents Receiving Chemotherapy
Nausea, Vomiting
About this trial
This is an interventional health services research trial for Nausea focused on measuring Nausea, Vomiting, Chemotherapy
Eligibility Criteria
Inclusion Criteria:
- All patients must have a histologically confirmed diagnosis of Osteosarcoma/ Malignant Fibrohistiocytoma of bone that is currently being treated with chemotherapy with high emetogenic potential chemotherapeutic agent(Cisplatin at a dose 120mg/m2 ; Adriamycin 75 mg/m2)
- Age group : 8-21 yrs.
- Weight : greater than or equal to 20 kg and less than 40 kg in Category 1
- Weight : greater than or equal to 40 kg and less than 60 kg in Category 2
- Patients who are willing to participate in study.
- Patients or their parents who can understand Hindi or English.
Exclusion Criteria:
- Patients of age <8 yrs or age >21 yrs.
- Weight < 20 kg and greater than or equal to 40 kg in Category 1
- Weight < 40 kg and greater than or equal to 60 kg in Category 2
- Patients receiving chemotherapy with drugs other than Cisplatin.
- Patients receiving a dosage of chemotherapy with Cisplatin<120 mg/m2.
Sites / Locations
- Dr. B.R. Ambedkar Institute Rotary Cancer HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Ginger arm
Placebo arm
The patients in this arm will be randomly selected in each cycle of chemotherapy. The unit of randomization is the cycle of chemotherapy. In each cycle of chemotherapy of all patients recruited in the study will be categorized using the computer generated random numbers. The patients in the ginger arm; Group A will be getting ginger powder capsules according to their body weight;ie;there are two weight categories within Group A: Category 1- 20kg-40kg Category 2- 40kg-60kg Category 1 will receive 2 capsules 3 times a day,ie; 1gram ginger powder per day Category 2 will receive 5 capsule divided in 3 doses per day,ie; 2gram ginger powder per day
Patients (children and adolescents) will be included in this arm after randomization of the cycle of chemotherapy of the patient. Starch powder/Glucose powder is used as placebo.The patients in the placebo arm; Group B will be getting ginger powder capsules according to their body weight;ie;there are two weight categories within Group B: Category 1- 20kg-40kg Category 2- 40kg-60kg Category 1 will receive 2 capsules 3 times a day,ie; 1gram placebo powder per day Category 2 will receive 5 capsule divided in 3 doses per day,ie; 2gram placebo powder per day