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Study identifier: NCT06540885 Synced from ClinicalTrials.gov · July 29, 2026
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A Comparison Between Palonosetron Versus Granisetron as PONV Prophylaxis in Scoliotic Patients Undergoing Spine Surgery

Condition: Postoperative Nausea and Vomiting · Scoliosis  ·  Sponsor: University of Malaya

PhasePhase 4
Planned participants74
Who can joinAll sexes, 10 Years to no upper limit
Healthy volunteersYes

About this study

The aim of this clinical trial is to compare the effectiveness of two Serotonin (5- HT3) receptor antagonist, palonosetron and granisetron, administered along with dexamethasone as a preventive measure against early and delayed postoperative nausea and vomiting (PONV) in adult and adolescent patients with idiopathic scoliosis (IS) undergoing posterior spinal fusion (PSF) surgery under total intravenous anesthesia (TIVA). The main questions the study aims to answer are: How effective is palonosetron compared to granisetron, when both combined with dexamethasone, in preventing PONV after scoliosis surgery? Are there any differences in the need for rescue antiemetics, occurrence of adverse effects related to the study drugs, and patient satisfaction between the two treatment groups? Participants in the study will be randomly assigned to receive either palonosetron or granisetron in addition to dexamethasone as part of their anesthesia and antiemetic regimen. The incidence and/ or severity of nausea, vomiting and retching will be assessed at 1 hour, 4 hours, 12 hours, 24 hours and 48 hours after surgery.

This description comes directly from the study's public registry record.

Talk to the study team

Kenlee Liew, MBBS  ·  +60195753579  ·  drkenliew@gmail.com

Siti Nadzrah Yunus, MAnaes, MBBS  ·  +60176975009  ·  siti.nadzrah@ummc.edu.my

Always discuss trial participation with your own doctor first.

Locations (2)

University MalayaPantai Valley, Kuala Lumpur, MalaysiaRecruiting
University Malaya Medical CentreKuala Lumpur, MalaysiaRecruiting

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Source record: clinicaltrials.gov/study/NCT06540885