An Open-label Trial of Clevidipine for Controlled Hypotension During Spinal Fusion

Completed · Phase 2/Phase 3

Conditions studied: Neuromuscular Scoliosis

In brief

The current study would prospectively evaluate the dosing requirements, efficacy and safety of clevidipine for controlled hypotension during spinal surgery in the pediatric population. As the investigators currently have projects underway which include those patients having scoliosis surgery for idiopathic scoliosis, this trial would include only those undergoing scoliosis surgery for neuromuscular disease.

Key facts

Study ID

NCT01645111

Run by

Nationwide Children's Hospital

People needed

50

Starts

2012-06-01

Expected to finish

2013-12-01

Last updated by the study team

2015-02-18

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Spinal fusion for neuromuscular scoliosis.

You may not qualify if…

• Allergy to dihydropyridine calcium channel antagonists
• Allergy to soy or eggs
• Non-neuromuscular causes of scoliosis
• Disorders of lipid metabolism (clevidipine is in a lipid base)

Where it is running

• Nationwide Children's Hospital — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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