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Effect of Prochlorperazine Combination with Standard Antiemetic Drug Regimen for Prevent Delayed Chemotherapy Induce Nausea and Vomiting in Oxaliplatin Based Regimen Chemotherapy, RCT Double Blind

Effect of Prochlorperazine Combination with Standard Antiemetic Drug Regimen for Prevent Delayed Chemotherapy Induce Nausea and Vomiting in Oxaliplatin Based Regimen Chemotherapy, RCT Double Blind

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210526005
Enrollment
86
Registered
2021-05-26
Start date
2021-06-13
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delayed Chemotherapy Induce Nausea and Vomiting in Oxaliplatin Based Regimen Chemotherapy CINV

Interventions

premedication before chemotherapy contain prochlorperazine 10 mg po bid combination with standard emetic regimen with dexamethasone 10 mg IV and ondansetron 8 mg IV maintainance phase in day 2-4 post-
Experimental Drug,Placebo Comparator Drug
prochlorperazine,placebo

Sponsors

medical oncology unit, Faculty of medicine, Chulalongkorn university
Lead Sponsor
Central Poly Trading Co., Ltd.
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. colorectal caner receiving 1st cycle of oxaliplatin based chemotherapy 2. not prior receive oxaliplatin 3. allow both palliative and curative intent 4. allow biologic agent such as antiVEGR antiEGFR

Exclusion criteria

Exclusion criteria: 1. history of bowel obstruction 2. nausea/vomiting symptom before receive chemotherapy 3. drug allergy of prochlorperazine, ondansetron, dexamethasone 4. abnormal liver or renal function 5. have psychotic problem 6. have history of seizure and dyskinesia 7. QT prolongation

Design outcomes

Primary

MeasureTime frame
complete response in delayed phase within 5 day after intervention proportion

Secondary

MeasureTime frame
complete response in acute phase and overall phase within 5 days proportion,complete controlled in acute, delay and overall phase within 5 days proportion,nausea severity within 5 days visual analog scale ,adverse effect within 5 days patient report outcome,patients preference end of study proportion

Countries

Thailand

Contacts

Public Contactpitan wongkongkathep

Faculty of medicine, Chulalongkorn university

nahtip@hotmail.com0813463814

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026