Dexmedetomidine for Reversal of Cocaine's Effects on the Heart
Completed · Early Phase 1
Conditions studied: Chest Pain, Acute Coronary Syndrome
In brief
This study will use myocardial contrast echocardiography performed during a continuous intravenous infusion of Definity microbubbles (Perflutren lipid microbubbles) to determine if dexmedetomidine (an intravenous central sympatholytic drug) can reverse all the cardiovascular effects of low-dose intranasal cocaine-including vasoconstriction in the coronary microcirculation-both in cocaine-naïve and non-treatment seeking cocaine-addicted subjects.
Key facts
- Study ID
- NCT01927640
- Run by
- Cedars-Sinai Medical Center
- People needed
- 115
- Starts
- 2013-02-01
- Expected to finish
- 2014-01-15
- Last updated by the study team
- 2020-01-14
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy adult subjects ages of 18-65 years without any history of substance abuse (other than tobacco), including narcotics, abuse of prescription painkillers, cocaine or any other recreational drug
You may not qualify if…
- Known or suspected right-to-left, bi-directional, or transient right-to-left cardiac shunts or detected by screening echocardiogram performed prior to I.V. infusion of Definity microbubbles
- Hypersensitivity or prior reactions to Definity microbubbles
- Pregnant or nursing women
- Any evidence of cardiopulmonary disease by history or physical examination, including subjects who are taking any cardiovascular medications of any sort
- History of hypertension or BP at time of consent > 140/90 mm Hg
- Any history of substance abuse (other than tobacco), including narcotics, prescription painkillers, cocaine or any other recreational drug (any person that says they have EVER tried these drugs will be excluded from this study)
- Subjects reporting alcohol intake of more than 2 drinks/day
- Severe psychiatric illness (e.g., schizophrenia, suicidal depression) in addition to drug dependence, which may signify a high risk of addiction
- Diabetes mellitus or any other systemic illness
- Individuals with a history of pseudocholinesterase deficiency
- Hypersensitivity to dexmedetomidine or lorazepam
- The presence of alcohol by breathalyzer
- Subjects who have poor echocardiography images will be screen failed.
- Persons with mechanically, magnetically, or electrically activated implants, such as cardiac pacemakers, neurostimulators, and infusion pumps (MRI only).
- Persons with ferromagnetic implants and ferromagnetic foreign bodies, such as intracranial, aneurysm clips, shrapnel and intraocular metal chips as these could become dislodged (MRI only).
- Persons unable to tolerate MRI imaging secondary to an inability to lie supine or severe claustrophobia (MRI only).
- Persons whose renal function test does not meet CSMC standard of care MRI contrast protocol requirements (GFR <45ml/min).
- Persons with allergy to animal dander or animal-instigated asthma
- Persons with a history of kidney or liver disease.
Where it is running
- Cedars-Sinai — Los Angeles, California, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.