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Validation of a Pediatric-Specific Abstinence Syndrome Assessment Tool

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2009 by Banner Health.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Banner Health
ClinicalTrials.gov Identifier:
NCT00792415
First received: November 17, 2008
Last updated: April 23, 2010
Last verified: December 2009
History of Changes
  Purpose

The purpose of this study is to assess the validity and reliability of an abstinence syndrome assessment tool used in pediatric patients with iatrogenic opioid dependence.


Condition
Substance Withdrawal Syndrome

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Validation of a Pediatric Abstinence Syndrome Scoring Tool Utilizing a Standardized Hospital-Based Guideline for Iatrogenic Opioid Dependence

Further study details as provided by Banner Health:

Primary Outcome Measures:
  • Total scores of abstinence syndrome symptoms [ Time Frame: Up to 23 days ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Expert opinion on abstinence syndrome [ Time Frame: Up to 23 days ] [ Designated as safety issue: No ]

Estimated Enrollment: 75
Study Start Date: November 2009
Estimated Study Completion Date: December 2010
Estimated Primary Completion Date: April 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts
1
Limited continuous opioid exposure (at least 120 and less than 156 hours)
2
Extended continuous opioid exposure (156 hours or more)

  Eligibility

Ages Eligible for Study:   up to 18 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Pediatric Intensive Care Unit patients

Criteria

Inclusion Criteria:

  • Pediatric Intensive Care Unit patients ages 2 weeks to 18 years
  • Patients receiving continuous opioid infusions for 5 days (at least 120 hours) or more

Exclusion Criteria:

  • Attending discretion
  • Patients with deterioration of medical status requiring interventions of pain control, surgery, sedation, or re-intubation
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00792415

Contacts
Contact: Teri Reyburn-Orne, RN, MSN, PNP 480-512-3373 teri.reyburn-orne@bannerhealth.com

Locations
United States, Arizona
Cardon Children's Medical Center Recruiting
Mesa, Arizona, United States, 85202
Contact: Teri Reyburn-Orne, RN, MSN, PNP     480-512-7901     teri.reyburn-orne@bannerhealth.com    
Sub-Investigator: Tarek Youssef, MD, FAAP            
Sub-Investigator: Stephanie Nevins, MD            
Sub-Investigator: Keith Reitzel, MD            
Sub-Investigator: Rima Abdouni, PharmD            
Sponsors and Collaborators
Banner Health
Investigators
Principal Investigator: Teri Reyburn-Orne, RN, MSN, PNP Banner Children's Hospital at Banner Desert Medical Center
  More Information

No publications provided

Responsible Party: Teri Reyburn-Orne, RN, MSN, CPNP-AC/Pediatric Pain Team Program Manager, Cardon Children's Medical Center
ClinicalTrials.gov Identifier: NCT00792415     History of Changes
Other Study ID Numbers: BHRI#05-08-0074
Study First Received: November 17, 2008
Last Updated: April 23, 2010
Health Authority: United States: Institutional Review Board

Keywords provided by Banner Health:
Abstinence syndrome symptoms
Withdrawal symptoms
Opioid dependence

Additional relevant MeSH terms:
Substance Withdrawal Syndrome
Substance-Related Disorders
Mental Disorders
Analgesics, Opioid
Analgesics
Sensory System Agents
 Peripheral Nervous System Agents
Physiological Effects of Drugs
Pharmacologic Actions
Central Nervous System Agents
Therapeutic Uses
Central Nervous System Depressants

ClinicalTrials.gov processed this record on May 16, 2013