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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

TypeNameDescription
DRUGSufentanilsufentanil 150μg, intravenous administration during post-operative 72 hours.
DRUGdexmedetomidine 1dexmedetomidine 0.05μg/kg/h, Continuous intravenous injection for 72 hours after operation
DRUGdexmedetomidine 2dexmedetomidine 0.1μg/kg/h, Continuous intravenous injection for 72 hours after operation
DRUGdexmedetomidine 3dexmedetomidine 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.