Clinical Trials Directory

Trials / Completed

CompletedNCT06423807

Preoperative Ondansetron Lozenge for Prevention of Post-Spinal Shivering in Caesarean Section

Preoperative Ondansetron Lozenge for Prevention of Post-Spinal Shivering in Caesarean Section: A Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Tanta University · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to estimate the role of ondansetron lozenge on prevention of post-spinal shivering in cesarean section.

Detailed description

Spinal anesthesia (SA) is preferred for cesarean section (CS) compared with general anesthesia(GA) because of several advantages, including prevention of the potential risk of GA-related neurotoxicity. Post-spinal shivering (PSS) could be a provocative factor for postoperative pain and its appropriate treatment prevents non-thermoregulatory tremors. Shivering also causes aggravating postoperative pain by stretching of sutures. Ondansetron is a selective antagonist for receptor 5-hydroxytryptamine 3 and is very effective in the prevention and treatment of shivering intra- and post-operation. Ondansetron can affect the body temperature and shivering in rats since the balance of nor-epinephrine and 5-hydroxytryptamine (5-HT) in the preoptic-anterior hypothalamus controls the temperature set point.

Conditions

Interventions

TypeNameDescription
DRUGOndansetron lozengePatients will receive ondansetron lozenge 4 mg (Ondalenz ©), 2 hours before surgery.

Timeline

Start date
2024-05-21
Primary completion
2024-09-29
Completion
2024-09-29
First posted
2024-05-21
Last updated
2024-10-08

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06423807. Inclusion in this directory is not an endorsement.