Trials / Completed
CompletedNCT05876039
Optimal Dosage of Remifentanil for Vertebroplasty
Comparison of Two Dosage of Remifentanil Infusion Combined With Propofol-based Total Intravenous Anesthesia in Percutaneous Vertebroplasty
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Tri-Service General Hospital · Academic / Other
- Sex
- All
- Age
- 20 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Percutaneous vertebroplasty has become a mainstay in the management of osteoporotic and malignant vertebral fractures. Procedural analgesia and sedation (PAS) with propofol and remifentanil may provides optimal hypnotic and analgesic effects.
Detailed description
Percutaneous vertebroplasty has become a mainstay in the management of osteoporotic and malignant vertebral fractures. Many anesthetic methods have been used in percutaneous vertebroplasty; however, there is no gold-standard method. Procedural analgesia and sedation (PAS) are one of the commonly used approaches. For its unique properties, including rapid onset, precise intraoperative control, and a fast recovery profile, remifentanil is preferable to other opioids administration in a target-controlled infusion (TCI) pump. Combination of remifentanil with propofol may improve sedation experience; however, it can increase a risk of respiratory depression. Moreover, propofol and remifentanil are often administered with 2 TCI pumps to, respectively, provide hypnotic and analgesic effects, which together are considered to be an ideal anesthetic technique.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Initial remifentanil effect-site concentration | Different initial remifentanil effect-site concentration |
Timeline
- Start date
- 2023-05-20
- Primary completion
- 2024-08-24
- Completion
- 2024-12-27
- First posted
- 2023-05-25
- Last updated
- 2025-01-08
Locations
1 site across 1 country: Taiwan
Source: ClinicalTrials.gov record NCT05876039. Inclusion in this directory is not an endorsement.