IRCT20090613002027N14
Completed
Phase 2
Evaluation of the efficacy and safety of adding olanzapine to the standard preventive regimen for chemotherapy- induced nausea and vomiting in children of 4-18 years of age, a Randomized Clinical Trial
Sari University of Medical Sciences0 sites49 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Palliative care.
- Sponsor
- Sari University of Medical Sciences
- Enrollment
- 49
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Cognitive abilities of 4 years old age
- •Receiving chemotherapy medications with moderate to severe risk of emesis
- •Age between 4 to 18 years old
Exclusion Criteria
- •Brain tumor
- •Receive of any anti psychotics 30 days before enrollment
- •Inhibitors/Inducers of CYP1A2
- •History of neuroleptic malignant syndrome
- •History of seizure
- •Sensitivity to olanzapine
- •Cardiac arrhythmia
- •History of uncontrolled diabetes mellitus
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
Investigation of efficacy and safety of add-on therapy with DPP-4 inhibitor in type 2 diabetic patients poorly controlled with basal supported oral therapyType 2 diabetesJPRN-UMIN000010849Department of Metabolism & Endocrinology Juntendo University Graduate School of Medicine40
Not yet recruiting
Phase 3
Effectiveness of Unani add-on therapy in preventing the disease severity of COVID-19 infectioHealth Condition 1: B972- Coronavirus as the cause of diseases classified elsewhereHealth Condition 2: J09- Influenza due to certain identified influenza virusesCTRI/2020/12/029575Central Council for Research in Unani Medicine
Recruiting
Phase 2
Evaluation of the efficacy and safety of lacosamide to duloxetine in the treatment of taxanes- induced peripheral neuropathyTaxane-induced neuropathy.IRCT20090613002027N21Mazandaran University of Medical Sciences60
Active, not recruiting
Not Applicable
A trial, in which subjects with type 2 diabetes, who qualify for treatment intensification, are given insulin degludec and, additionally, either liraglutide or insulin aspart, both in combination with metformin, with the largest meal. The purpose is to compare efficacy and safety of these two treatments.EUCTR2011-001493-25-ATovo Nordisk A/S420
Active, not recruiting
Not Applicable
A trial, in which subjects with type 2 diabetes, who qualify for treatment intensification, are given insulin degludec and, additionally, either liraglutide or insulin aspart, both in combination with metformin, with the largest meal. The purpose is to compare efficacy and safety of these two treatments.Type 2 diabetesMedDRA version: 14.0Level: LLTClassification code 10045242Term: Type II diabetes mellitusSystem Organ Class: 10027433 - Metabolism and nutrition disordersTherapeutic area: Diseases [C] - Nutritional and Metabolic Diseases [C18]EUCTR2011-001493-25-DEovo Nordisk A/S420