Clinical trial · Interventional
Patient Satisfaction, Efficacy and Compliance of Antiemetic Patch vs Pill in Malignant Glioma Patients
Phase II Randomized Cross-over Study to Evaluate Patient Satisfaction, Efficacy and Compliance of Granisetron Patch vs. Ondansetron in Malignant Glioma Patients Receiving Standard Radiotherapy (RT) and Concomitant Temozolomide (TMZ)
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Lack of approval and funding from company
Summary
Brief summary (as posted)
The purpose of this study is to assess patient satisfaction, the efficacy and compliance of granisetron patch versus ondansetron pills for radiation induced nausea and vomiting in malignant glioma patients receiving six weeks of radiation therapy (RT) and concomitant temozolomide (TMZ). Use of the patch may benefit brain tumor patients by increasing compliance. All eligible adult malignant glioma subjects should receive a planned total dose of 54-60 GY of radiation and 75 mg/m2 of daily TMZ for a total of six weeks. Subjects will be randomized to receive either granisetron patch or ondansetron for three weeks. Weeks 3-6, they will received the other medication. The granisetron transdermal delivery system (supplied as a 52 cm\^2 patch containing 34.3 mg of granisetron - 3.1 mg/day) is applied once per week 24 hours before the weekly radiation and chemotherapy, while the ondansetron 8 mg oral tablet is taken once a day 30-60 minutes prior to each dose of chemotherapy. Subjects will fill out questionnaires regarding the effectiveness of the medication and their satisfaction, and which anti-emetic they prefer. Safety will be assessed throughout the six weeks of radiation by the clinical research nurse using the Common Toxicity Criteria for Adverse Events (CTCAE), version 4.0. All subjects who receive both ondansetron and Granisetron Transdermal Delivery System (GTDS) treatment will be included in analyses of treatment preference. However, all other efficacy and safety analyses will include all subjects who received ondansetron or GTDS.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Malignant Glioma | Malignant Glioma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Granisetron | Drug | — | UNRESOLVED |
| Ondansetron | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Granisetron patch
- description
- Granisetron transdermal delivery system (supplied as a 52 cm\^2 patch containing 34.3 mg of granisetron - 3.1 mg/day) is applied once per week.
- interventionNames
- Drug: Granisetron
- type
- ACTIVE_COMPARATOR
- label
- Ondansetron tablet
- description
- Ondansetron 8 mg oral tablet is prescribed for once a day.
- interventionNames
- Drug: Ondansetron
Primary outcomes (1)
- measure
- Satisfaction with Granisetron Transdermal Delivery System (GTDS) versus Ondansetron pill
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients must have histologically confirmed diagnosis of malignant glioma (Glioblastoma, gliosarcoma or anaplastic astrocytoma, or anaplastic oligodendroglioma) who may or may not be chemotherapy naïve and who are scheduled to receive radiotherapy (for a total of 60 GY) and concomitant daily temozolomide therapy (at a dose of 75 mg/m2 for one complete six week cycle). 2. Age ≥ 18 years 3. Karnofsky ≥ 60% 4. Hematocrit \> 29%, ANC \>1,000 cells/mm3, platelets \> 100,000 cells/ mm3 5. Serum creatinine \< 1.4 mg/dl, serum SGOT and bilirubin \< 1.5 times upper limit of normal 6. For patients on corticosteroids, they must have been on a stable dose for 1 week prior to entry, and the dose should not be escalated over entry dose level, if clinically possible 7. Ability and willingness to give informed consent 8. If sexually active, patients will take contraceptive measures for the duration of the treatments 9. Negative serum pregnancy test 48 hours prior to beginning study drug Exclusion Criteria: 1. Pregnancy or breastfeeding 2. Co-medication that may interfere with study results; e.g., immune-suppressive agents other than corticosteroids 3. Inability or unwillingness to cooperate with the study procedures 4. Prophylactic medication for the prevention of nausea and vomiting 24 hours prior to the start of radiation therapy through the full course of radiation therapy is prohibited, with the exception of the study drug. Corticosteroids will be allowed for treatment of cerebral swelling. Rescue medication for treatment of nausea and vomiting is permitted after radiation therapy at the discretion of the investigator 5. Previous participation in any clinical trial involving granisetron 6. Any vomiting, retching, or NCI Common Toxicity Criteria version 4.0 grade 2-4 nausea in the 24 hours preceding radiation and chemotherapy 7. Ongoing vomiting from any organic etiology 8. Radiotherapy of abdomen within one week prior to or during the study 9. Received granisetron within 14 days prior to study enrollment 10. Prior and concomitant cancer chemotherapy and radiotherapy
References
Publications (0)
Data not yet available