Remifentanil Versus Morphine for Sedation of Premature Neonates With Respiratory Distress Syndrome
Information source: Federal University of Minas Gerais
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Respiratory Distress Syndrome
Intervention: Remifentanil (Drug)
Phase: Phase 4
Status: Completed
Sponsored by: Federal University of Minas Gerais Official(s) and/or principal investigator(s): Yerkes P Silva, MD, MSc, Principal Investigator, Affiliation: Faculty of Medicine from Federal University of Minas Gerais
Summary
In this randomised controlled study we intended to compared intubation conditions and the
continuous infusion of remifentanil (n=10) and morphine (n=10) in mechanically ventilated
premature neonates (28-34wk) regarding the time to be awake and, the time until extubation
after interruption of the opioid administration.
Clinical Details
Official title: Comparative Study of the Use of Remifentanil Versus Morphine for Sedation and Analgesia of Premature Neonates During Mechanical Ventilation in the Treatment of Respiratory Distress Syndrome (RDS)
Study design: Supportive Care, Randomized, Double-Blind, Active Control, Parallel Assignment
Primary outcome: Intubation conditions using a four point scaleDecrease in time after interruption of sedation until the neonate be awake. Decrease in time after interruption of sedation until the neonate be extubated.
Secondary outcome: Pain and stress before and after intubation (NIPS and Comfort scores).Pain and stress during continuous infusion of remifentanil versus morphine during mechanical ventilation for the treatment of respiratory distress syndrome (NIPS and Comfort scores).
Detailed description:
Intubation and mechanical ventilation are majors component of intensive care for premature
neonates with respiratory distress syndrome (RDS) and is associated with physiologic,
biochemical, and clinical responses indicating pain and stress in prematures. Although
morphine is one of the most used drugs for premedication and for sedation and analgesia
during mechanical ventilation in the treatment of RDS its pharmacological profile precludes
several limitations mostly due to its much delayed onset of action what makes the drug not
suitable as premedication and due to its prolonged duration of action mainly in prematures.
Unlike morphine, remifentanil has an unique pharmacokinetic properties with a rapid onset of
action and, a fast decrease in plasma concentration after interruption of administration due
to a context-sensitive half-time of 3. 2 minutes. So, it could be the ideal opioid for
neonates who are especially sensitive to respiratory depression by opioids
Eligibility
Minimum age: N/A.
Maximum age: 28 Days.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Gestational age between 28 and 34 wk
- Clinical and radiological features compatible with respiratory distress syndrome that
required an elective tracheal intubation and surfactant therapy.
Exclusion criteria:
- The presence of major congenital malformations
- Birth weigh less than 1000g
- Previous or concurrent use of opioid for any reason (cesarean section with general
anaesthesia)
- Hemodynamic instability before the indication of tracheal intubation
- Refuse of the parents to enroll the neonate in the study protocol
Locations and Contacts
Additional Information
Related publications: Pereira e Silva Y, Gomez RS, Barbosa RF, Simoes e Silva AC. Remifentanil for sedation and analgesia in a preterm neonate with respiratory distress syndrome. Paediatr Anaesth. 2005 Nov;15(11):993-6.
Starting date: April 2004
Ending date: November 2005
Last updated: October 19, 2006
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