Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
12 participants
OBSERVATIONAL
2011-09-30
2013-09-30
Brief Summary
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Detailed Description
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Obesity has also become an important challenge for the anesthesiologist. Safety and drug dosing particularly within the field of pediatric anesthesia, is of paramount concern as it can affect patient outcomes. Data collected in the United Kingdom from more than 100,000 anesthetized pediatric patients showed that a critical incident is twice as likely to occur in an obese child in the preoperative period as in an obese adult. A possible explanation may be linked to the lack of precision in drug dosing for these obese patients.
Fentanyl is a frequently used opioid analgesic in pediatric and adult anesthesia. Fentanyl is commonly administered to pediatric patients undergoing anesthesia as it is has a high potency, a rapid onset and a short duration of action. Due to these properties intravenously administered fentanyl is well suited as an analgesic compound in general anesthesia in pediatric patients.
The pharmacokinetics of fentanyl in adults have been well documented. Although there are some studies investigating the pharmacokinetic properties of oral, transmucosal and intravenous fentanyl preparations in children, the disposition of fentanyl in pediatric patients has not been sufficiently described. Several studies in infants and children report age-dependent differences in the pharmacokinetic/ pharmacodynamic parameters of intravenously administered fentanyl.
Currently there are no data available about the pharmacokinetics/ pharmacodynamics of fentanyl in adolescent obese patients.
Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Fentanyl use for surgical pain
Adolescent patient having surgery
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2\. The BMI will be calculated using height and weight and will include the 5th to 84th percentile for the control group and greater than or equal to 95th percentile for the obese adolescents.
3\. All racial and ethnic groups will be included.
Exclusion Criteria
2. Prior exposure to any opioid including fentanyl within a 24 hour period.
3. Patients with known hypersensitivity to any opioids.
4. History of central nervous system dysfunction and active upper airway disease and liver and renal disease. Patients diagnosed with renal or liver disease as evidenced by abnormal function tests within the past 12 months will be excluded.
5. Patients who are treated with drugs known to affect the cytochrome P450 3A (CYP3A4), like antiepileptics, imidazole derivates, macrolides, corticosteroids and grapefruit juice
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12 Years
20 Years
ALL
Yes
Sponsors
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Children's National Research Institute
OTHER
Responsible Party
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Janelle Vaughns
Assistant Professor, Anesthesiology and Perioperative Medicine
Principal Investigators
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John van den Anker, MD
Role: PRINCIPAL_INVESTIGATOR
Children's National Research Institute
Locations
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Childrens National Medical Center
Washington D.C., District of Columbia, United States
Countries
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References
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Vaughns JD, Ziesenitz VC, Williams EF, Mushtaq A, Bachmann R, Skopp G, Weiss J, Mikus G, van den Anker JN. Use of Fentanyl in Adolescents with Clinically Severe Obesity Undergoing Bariatric Surgery: A Pilot Study. Paediatr Drugs. 2017 Jun;19(3):251-257. doi: 10.1007/s40272-017-0216-6.
Other Identifiers
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1809
Identifier Type: -
Identifier Source: org_study_id