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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 scale

Decrease 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

Page last updated: June 20, 2008

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