Overview
Dexmedetomidine for Immediate Perioperative Analgesia in Pediatric Patients Undergoing Tonsillectomy
Status:
Completed
Completed
Trial end date:
2008-10-01
2008-10-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The primary purpose of this study is: 1. To compare dexmedetomidine with fentanyl in terms of intra-operative hemodynamics and post-operative analgesia. 2. To determine an analgesic dose response relationship for dexmedetomidine. 3. Compare recovery characteristics of dexmedetomidine to fentanyl.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Children's National Research Institute
Children's Research InstituteCollaborators:
Hospira, Inc.
Hospira, now a wholly owned subsidiary of PfizerTreatments:
Dexmedetomidine
Fentanyl
Criteria
Inclusion Criteria:- All of the following criteria must be met for the potential subject to be eligible for
participation:
1. The subject is 2 to 12 years of age
2. The subject's American Society of Anesthesiologists physical status is ASA I or
II (see appendix 1).
3. The subject is scheduled for elective tonsillectomy with or without adenoidectomy
surgery (procedures with myringotomy tube placement are allowed).
4. The subject will be hospitalized overnight after surgery
5. The subject's parent/legally authorized guardian has given written informed
consent to participate; and where applicable, the subject has given appropriate
assent to participate.
Exclusion Criteria:
- The potential subject is NOT eligible for participation if any of the following
exclusion criteria apply:
1. The subject has a history or a family (parent or sibling) history of malignant
hyperthermia
2. The subject has known significant renal or hepatic disorders determined by
medical history, physical examination or laboratory tests.
3. The subject has a known or suspected allergy to opioid analgesics
4. The subject is a pregnant or lactating female (if post-menarcheal, a negative
pregnancy test must be confirmed prior to the planned surgery time (in AMSAC)
consistent with current standard of care.
5. The subject has history of. cardiovascular issues which would preclude the use of
dexmedetomidine, (e.g. Down's Syndrome, dysrhthymias, conditions where
hypotension is to be avoided).