Trials / Unknown
UnknownNCT02552459
Effect of Dexmedetomidine Combined With Sufentanil for Postoperative Intravenous Analgesia in Neurosurgery
Effect of Dexmedetomidine Combined With Sufentanil for Postoperative Intravenous Analgesia in Neurosurgery: A Randomized Controlled Study
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 120 (estimated)
- Sponsor
- First Affiliated Hospital, Sun Yat-Sen University · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine effect of combined medication of sufentanil and dexmedetomidine in patient controlled analgesia after neurosurgery.
Detailed description
Sufentanil is a classical drug for postoperative analgesia. Dexmedetomidine is a commonly used α2-adrenergic receptor, and it helps provide sedation, analgesia and inhibition of sympathetic activation. The investigators propose to recruit 120 patients who is undergoing the arteriovenous malformation embolism operation in department of Neurosurgery. Patients will be randomly divided into 4 groups(control group, sufentanil and low dexmedetomidine dose group, sufentanil and middle dexmedetomidine dose group, sufentanil and high dexmedetomidine dose group), then the investigators select post-operative records to determine whether dexmedetomidine can take a positive role in neurosurgical analgesia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Sufentanil | sufentanil 150μg, intravenous administration during post-operative 72 hours. |
| DRUG | dexmedetomidine 1 | dexmedetomidine 0.05μg/kg/h, Continuous intravenous injection for 72 hours after operation |
| DRUG | dexmedetomidine 2 | dexmedetomidine 0.1μg/kg/h, Continuous intravenous injection for 72 hours after operation |
| DRUG | dexmedetomidine 3 | dexmedetomidine 0.15μg/kg/h, Continuous intravenous injection for 72 hours after operation recorded in the following 72h. |
Timeline
- Start date
- 2015-09-01
- Primary completion
- 2016-12-01
- Completion
- 2016-12-01
- First posted
- 2015-09-17
- Last updated
- 2016-10-18
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT02552459. Inclusion in this directory is not an endorsement.