Skip to main content
Clinical Trials/CTRI/2025/05/086615
CTRI/2025/05/086615Not yet recruitingPhase 2/3

Study to evaluate the antiemetic efficacy of ginger root extract capsules for children adolescents and young adults receiving highly emetogenic chemotherapy A Seamless Placebo controlled single centre combined Phase II and III Randomized Controlled Trial

HIMALAYA WELLNESS COMPANY1 site in 1 country538 target enrollmentStarted: January 6, 2025Last updated:
Conditions

Trial Snapshot

Phase
Phase 2/3
Status
Not yet recruiting
Enrollment
538
Locations
1
Primary Endpoint
Phase II study: To identify the best dose of ginger-root-extract-capsules for the phase III trial based on a decrease in chemotherapy-induced nausea (mean PeNAT scale score) for children, adolescents, and young adults (6 to 21 years) receiving HEC as compared to placebo.

Study Overview

Brief Summary

Chemotherapy-induced nausea and vomiting (CINV) affects 40–70% of pediatric patients—over twice the risk seen in adults—despite antiemetic prophylaxis, which can reduce treatment adherence and increase hospitalization costs. Current guidelines recommend 5-HT3 receptor antagonists and dexamethasone for acute CINV in children, but research on pediatric cases remains limited, and no standard guidelines exist for delayed CINV. This highlights the need for additional or alternative treatments to manage CINV in children, adolescents, and young adults effectively. In a double-blind placebo-controlled trial, we have previously demonstrated that ginger-root-extract-capsules improve nausea and vomiting for children receiving cisplatin-containing chemotherapy. Several trials have demonstrated the efficacy of ginger in preventing CINV in adults. However, the proper dose and standardization of formulation are not yet well explored, and there is a lack of enough evidence to suggest statistically significant benefits in children, adolescents, and young adults.

There is a notable lack of research and well-conducted clinical trials on effective interventions for managing CINV in pediatric oncology. This study aims to bridge this gap by investigating the use of ginger capsules to alleviate nausea and vomiting in children, adolescents, and young adults receiving highly emetogenic chemotherapy. As a widely available, safe, and well- tolerated natural remedy, ginger offers a good option. This trial seeks to evaluate its efficacy in preventing CINV in children, adolescents, and young adults, adolescents, and young adults. If proven effective, ginger-root-extract-capsules could become a cost-effective, accessible, and practical option for managing CINV.

Study Design

Study Type
Interventional
Allocation
Adaptive randomization, such as minimization
Masking
Participant and Investigator Blinded

Eligibility Criteria

Ages
6.00 Year(s) to 21.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Body weight greater then equal to 15kg Diagnosis of solid or hematological malignancy scheduled to receive any cycle of a highly emetogenic chemotherapy regimen.

Exclusion Criteria

  • •CNS neoplasm primary or secondary (except vertebral or skull metastasis as long as they are not breaching dura or compressing brain/spinal cord parenchyma) Vomiting or retching within 24 hours before receipt of chemotherapy Use of systemic steroids for malignancy or other uncontrolled systemic disease Severe organ damage based on laboratory investigation within 2 weeks at the time of screening Hepatic transaminitis greater then equal to 5 times upper limit normal and or serum bilirubin greater then equal to 3 times upper limit normal of reference laboratory Renal serum creatinine greater then equal to 1.5 times upper limit normal of reference laboratory Any clinical evidence of heart failure Uncontrolled bleeding manifestation known coagulopathy and patients on anticoagulation therapy Receipt of radiation to abdomen cranium or pelvis (within 1 week) Not able to read Hindi or English Not able to swallow capsules Refusal to provide consent.

Outcomes

Primary Outcomes

Phase II study: To identify the best dose of ginger-root-extract-capsules for the phase III trial based on a decrease in chemotherapy-induced nausea (mean PeNAT scale score) for children, adolescents, and young adults (6 to 21 years) receiving HEC as compared to placebo.

Time Frame: Phase II study: 21 days for each participant | Phase III study: 21 days for each participant

Phase III study: To examine the efficacy of the best dose of the ginger-root-extract-capsules identified in the phase II trial on the incidence of complete remission (CR) in chemotherapy-induced vomiting (CIV) in the acute phase compared to placebo among children, adolescents, and young adults receiving HEC.

Time Frame: Phase II study: 21 days for each participant | Phase III study: 21 days for each participant

Secondary Outcomes

  • a.Incidence of CR in CIV in delayed and overall phase(b.The severity of chemotherapy-induced nausea (by PeNAT score) in both arms)

Investigators

Sponsor Class
Pharmaceutical industry-Indian

Study Sites (1)

Loading locations...

Similar Trials