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
| Type | Name | Description |
|---|---|---|
| DRUG | Ondansetron lozenge | Patients 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.