Clonidine to Treat Iatrogenic-induced Opioid Dependence in Infants
Neonatal Abstinence Syndrome
Drug: Clonidine HCL
|Study Design:||Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
|Official Title:||Efficacy of Clonidine in Reducing Iatrogenic-induced Opioid Dependence in Infants:|
- Time to complete detoxification [ Time Frame: 2-4 weeks ] [ Designated as safety issue: No ]Time to complete detoxification is defined as 48 hrs off all opioids/benzodiazepines and study drug with acceptable withdrawal scores of <9 (on average we expect the infant to be enrolled in the study for 2-4 weeks).
- Cardiovascular side-effects changes HR and BP [ Time Frame: 48 hrs after starting study drug and for 48hrs after stopping study drug ] [ Designated as safety issue: Yes ]Changes in HR and BP for 48 hrs after starting study drug and for 48hrs after stopping study drug
- Cumulative dose of opioid and benzodiazepine [ Time Frame: 2-4 weeks ] [ Designated as safety issue: No ]We will determine the total amount of opioid and benzodiazepine needed from the start of detoxification to the end of the the detoxification.
|Study Start Date:||July 2011|
|Estimated Study Completion Date:||December 2014|
|Primary Completion Date:||July 2011 (Final data collection date for primary outcome measure)|
Infants will receive intravenous or oral clonidine(Duraclon) for the treatment of pain and sedation
Drug: Clonidine HCL
At day 5 on opioid and/or benzodiazepine (BZD), the infant will be randomized to receive either placebo (normal saline) or clonidine 1μg/kg/q 4 hrs to a maximum dose of 2μg/kg/q 4. Weaning from the study drug: When the opioid is no longer required, 24 hrs later the study drug (placebo or study drug) will be reduced by 50% and then discontinued 24 hours later provided that the Modified Finnegan scores remain between < 9.
Other Name: Duraclon
Placebo Comparator: Control
Infants will receive place (saline) (if receiving it IV) or orally (sterile water) if receiving it orally
Infants randomized to placebo will be administered IV saline or oral sterile water in the same volume as study drug. The placebo will be give every 4 hrs as outlined in the algorithm for the study.
Other Name: placebo, sterile water, saline
The study will test the following 2 specific aims:
Specific Aim 1
To determine the efficacy and short-term safety of clonidine in reducing the severity of iatrogenic neonatal abstinence syndrome (NAS) by decreasing the time required for complete sedative and analgesic drug detoxification. The investigators will enroll 88 neonates at risk for having moderate to severe NAS in a randomized, double-blinded placebo controlled trial comparing opioid/benzodiazepine administration combined with a placebo (control) vs. opioid/benzodiazepine combined with clonidine. Principal outcome measure will be the difference in length of treatment for complete detoxification. Early safety of clonidine will be determined by monitoring for cardiorespiratory side effects that might be associated with clonidine use in this high risk population.
Specific Aim 2
To determine the pharmacokinetics and pharmacodynamics of clonidine in this critically ill infant population. The investigators will estimate the dose-exposure-response relationship of clonidine in neonates at risk for developing iatrogenic by using nonlinear mixed-effects population pharmacokinetic (PK)-pharmacodynamic (PD) analysis.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01360450
|United States, Maryland|
|Johns Hopkins Hospital|
|Baltimore, Maryland, United States, 21287|
|Principal Investigator:||Estelle B Gauda, MD||Johns Hopkins University|