Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06988124

Dexamethasone Palmitate for PONV After Craniotomy

Intravenous Dexamethasone Palmitate for Prophylaxis of Postoperative Nausea and Vomiting After Craniotomy

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
500 (estimated)
Sponsor
Beijing Tiantan Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Dexamethasone is almost one of the most commonly used drugs for postoperative nausea and vomiting (PONV) prevention. However, PONV is still a complex problem to be solved; for example, even with preoperative dexamethasone administration, there are still some patients undergoing craniotomy still experience PONV within 24 hours postoperatively. Compared to dexamethasone, dexamethasone palmitate has a long-lasting anti-inflammatory effect, 2-5 times that of traditional water-soluble dexamethasone, with fewer adverse effects. This trial aims to assess the effect and safety of preoperative dexamethasone palmitate on PONV after craniotomy.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasone PalmitatePatients in the dexamethasone palmitate group will be assigned to receive intravenous injection of dexamethasone palmitate 8 mg (contains 5mg dexamethasone) after anesthesia induction and before surgical incision.
DRUGDexamethasonePatients in the dexamethasone group will be assigned to receive intravenous injections of dexamethasone 5 mg after anesthesia induction and before surgical incision.

Timeline

Start date
2025-06-25
Primary completion
2027-05-01
Completion
2027-06-01
First posted
2025-05-23
Last updated
2025-09-23

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06988124. Inclusion in this directory is not an endorsement.