Nausea With Vomiting Chemotherapy-Induced

4

Review clinical trials related to Nausea With Vomiting Chemotherapy-Induced. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

BMT-08: A Comparative Effectiveness Study of Transdermal Granisetron to Ondansetron

Patients undergoing either an autologous or allogeneic hematopoietic stem cell transplant (HSCT) and receiving preparative chemotherapy experience a considerable amount of chemotherapy-induced nausea and vomiting (CINV). Current strategies at reducing CINV in this patient population are suboptimal due to lack of efficacy and supportive evidence, potential for increased adverse events, and drug-drug and drug-disease contraindications.

Participants needed: 90
Trial details
Phase: Phase 4Age: 18-75Biological sex: AllType: InterventionalSponsor: University of Illinois at ChicagoUpdated: Nov 12, 2025Locations: 1
Eligibility criteria

Age 18-75 years at time of enrollment receiving either a preparative regimen and... [+4]

Concurrent use of amifostine [+2]

Status: Recruiting

Implementation of Personalized Medicine for Optimal Drug Therapy in Cancer

A prospective longitudinal cohort study that will assess the effect of a Personalized Medicine (PM) clinic recommendations on pharmacogenetic variation and/or interacting drugs on plasma drug exposure, effectiveness or toxicity of commonly used antidepressant, pain, and antiemetic medications in cancer patients. Such recommendations will entail genotype-guided treatment suggestions while also considering potential DDI, and will be provided to patients during their clinic visit, and referring physicians thereafter. Drug concentration and therapeutic effectiveness will be assessed before (baseline) and 6 months after recommendations have been provided. To assess effectiveness, patient-reported outcomes will be evaluated using validated scales for symptoms of depression, pain and chemotherapy-induced nausea/ vomiting The investigators hypothesize that the pharmacogenetic variation and DDI, if applicable, determine steady state drug concentration and therapeutic response or toxicity of the investigated antidepressant, pain or antiemetic treatments at baseline, while there is a clinically significant reduction or absence of the effect 6 months after the PM clinic recommendations to referring physicians and patients.

Participants needed: 600
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph'sUpdated: Jul 9, 2025Locations: 1
Eligibility criteria

Age 18 years or older [+2]

Patients who are unable to complete study materials (surveys) with or without as... [+3]

Status: Not yet recruiting

Predict CHimio-or Radiation-induced NAusea and Vomiting in Children/adolescents Treated for Cancer

Chemo- or radiation-induced nausea and vomiting (CRVN) is one of the most frequent and feared side effects. It is a symptom that is few or not at all evaluated. There is a significant discrepancy between the perception of the CRVN symptom by caregivers and the patient's own experience. At present, there is no real consensus to manage CRVN with medication, and CRVN relief is also the subject of heterogeneous practices. The importance of primary prevention of CRVN, before starting the first treatment sequence, has been highlighted to optimize the action of antiemetic treatments and limit the risk of anticipated nausea and vomiting (NV). The investigators' objective is to objectively assess the risk of CRVN in children/adolescents treated for cancer (and thus effectively prevent this symptom).

Participants needed: 150
Trial details
Age: 4-18Biological sex: AllType: ObservationalSponsor: Rennes University HospitalUpdated: Mar 11, 2025Locations: 5
Eligibility criteria

Treated in a pediatric onco-hematology center in the GOCE (Grand Ouest Cancer En... [+3]

Patients or legal representatives with French understanding difficulties. [+1]

Status: Recruiting

Ondanstron Weekly vs Every 3 Weeks for Prevention of Nausea and Vomiting Induced by Chemotherapy Combined With PD-1 Blockade

The aim of this randomized study is to compare the efficacy and safety of ondanstron weekly with every 3 weeks for the prevention of nausea and vomiting induced by chemotherapy combined with PD-1 blockade.

Participants needed: 98
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hubei Cancer HospitalUpdated: Feb 29, 2024Locations: 1
Eligibility criteria

Age ≥ 18 years, no gender limit; [+8]

Nausea or vomiting caused by reasons except for chemotherapy and PD-1 blockade; [+4]