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CompletedNCT02454881

Dose Response Study of Dexmedetomidine in Orthopaedic Spine Surgery Patients

Dose Response Study of Patient Controlled Analgesia (PCA) of Dexmedetomidine in Orthopaedic Spine Surgery Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
107 (actual)
Sponsor
Turku University Hospital · Other Government
Sex
All
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

To study the multimodal protocol combining adjunct dexmedetomidine with oxycodone in intravenous patient-controlled analgesia bolus dosing and effects in patients scheduled for posterolateral lumbar spine fusion with bilateral transpedicular screw instrumentation.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidine
DRUGOxycodone

Timeline

Start date
2015-06-01
Primary completion
2019-10-31
Completion
2020-03-01
First posted
2015-05-27
Last updated
2020-09-22

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT02454881. Inclusion in this directory is not an endorsement.

Dose Response Study of Dexmedetomidine in Orthopaedic Spine Surgery Patients (NCT02454881) · Clinical Trials Directory