Multicenter, Randomized, Double-blind, Placebo Controlled, Study to Evaluate the Activity of a Ginger (Zingiber Officinale) Food Supplement in the Management of Nausea in Patients Receiving Highly Emetogenic Treatments and Standard Anti-emetogenic Therapy.
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Helsinn Healthcare SA
- Enrollment
- 250
- Locations
- 11
- Primary Endpoint
- To evaluate the efficacy of Ginger in protecting patients from delayed nausea (incidence of no delayed nausea and non-significant delayed nausea)
Study Overview
Brief Summary
The purpose of the study is verify the capability of a standardized Ginger (Zingiber officinale) extract to manage nausea in cancer patients receiving highly emetogenic treatments and standard anti-emetogenic therapy.
Detailed Description
This study is a randomized, double-blind, placebo controlled, multicenter study with two parallel groups of patients.
The study will be conducted in 5 Italian clinical sites and will involve 250 patients receiving at least 2 cycles of highly emetogenic treatments.
Patients will be randomly assigned to Ginger treatment or to its Placebo.
All patients will receive, at each chemotherapy cycle, the standard 5-HT3 receptor antagonist antiemetics plus dexamethasone and NK1 receptor antagonist. This will guarantee to all patients an antiemetic prophylaxis for acute and delayed nausea. No additional treatment is usually foreseen for nausea and this justifies the use of placebo in the control group.
Patients will start the study treatment on the day after chemotherapy cycle and will continue until the day of the following cycle; they will suspend the study treatment on the chemotherapy day and will start again on the next day. The choice not to treat the patients with the study product on the chemotherapy day is intended to avoid any possible interference with antiemetic therapy of the first day and chemotherapy, and to analyze the impact of Ginger in delayed phase without confounding factors in acute phase.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- Triple (Participant, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Male and Females aged > 18 years.
- •Naïve to chemotherapy.
- •Patients planned to receive at least 2 cycles of highly emetogenic treatments with cisplatin in single dose > 50 mg/m2 every 21 or 28 days.
- •Willing and able to understand and sign informed consent and complete the patient diary.
Exclusion Criteria
- •Presence of brain symptomatic metastases (in case of small, asymptomatic metastases and in absence of steroids treatment, the patient is eligible).
- •Scheduled to receive or having received in the past 4 weeks radiation treatment to brain, abdomen or pelvis.
- •Emesis or significant nausea within 24 hours before first chemotherapy cycle.
- •Known hypersensitivity reaction to Ginger or any components of the product.
- •Patients with coagulopathies causing potential increase risk of bleeding.
- •Patients on therapy with oral anticoagulants.
- •Planned surgery procedures in the period of the study or within 2 weeks after the study conclusion.
- •History of seizures.
- •Active use of cannabinoids.
- •Known current or past drug or alcohol abuse.
- •Use of other investigational drugs within 30 days before study entry or during the study.
- •Clinically significant findings on physical exam or presence of known clinically significant disease that would interfere with study evaluation
Outcomes
Primary Outcomes
To evaluate the efficacy of Ginger in protecting patients from delayed nausea (incidence of no delayed nausea and non-significant delayed nausea)
Time Frame: Two High Emetogenic chemotherapy cylces (41 or 55 days)
The level of nausea will be assessed through a Visual Analogue Scale (VAS 0-100 mm) included in the patients' daily diary. The patients will be asked to report the maximum level of nausea experienced during each day. During each chemotherapy cycle, the nausea occurring between day 2 and day 5 will be defined as "delayed nausea", the nausea occurring between day 6 and day 19/26 will be considered as "inter-cycle nausea". The day before the next chemotherapy cycle (day 20/27), "anticipatory nausea" symptoms will be collected.
Secondary Outcomes
- Protection from delayed vomiting (number of emetic episodes in delayed phase)(Two High Emetogenic chemotherapy cylces (41 or 55 days))
- Overall fatigue assessment (BFI questionnaire)(Two High Emetogenic chemotherapy cylces (41 or 55 days))
- Use of antiemetic rescue medication.(Two High Emetogenic chemotherapy cylces (41 or 55 days))