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A Comparison of Postoperative Tramadol Versus Acetaminophen With Codeine in Children Undergoing Tonsillectomy

Primary Purpose

Tonsillitis, Pain

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Codeine with acetaminophen
Tramadol suspension
Sponsored by
Children's Hospitals and Clinics of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tonsillitis focused on measuring Tonsillectomy, Pain, Pediatric, Opioids, Tramadol, Codeine

Eligibility Criteria

4 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Child must be scheduled to undergo tonsillectomy (with or without adenoidectomy).
  • Child must be between the ages of 4 and 15 at the time of enrollment.
  • Child and caregiver must be English-speaking.
  • The same caregiver (e.g., mother) must agree to complete all study assessments with child to ensure consistency.

Exclusion Criteria:

  • Child cannot self-assess pain due to conditions such as developmental delays, chromosomal abnormalities, and other syndromes.
  • Child had significant adverse effects to codeine, tramadol, or acetaminophen in the past.
  • Child has a known underlying seizure disorder (not febrile seizure).
  • Child has known underlying renal or liver dysfunction (with creatinine, aspartate aminotransferase [AST]/amino alanine transferase [ALT], above normal value for age, respectively).
  • Child or caregiver is not English-speaking.
  • The same caregiver (e.g., mother) is unable to complete all follow-up assessments.

Sites / Locations

  • Children's Hospitals and Clinics of Minnesota

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Capital® with Codeine Suspension

Tramadol suspension

Arm Description

Outcomes

Primary Outcome Measures

Efficacy of Two Different Liquid Pain Medications: Tramadol vs. Codeine/Acetaminophen During the Post-tonsillectomy Recovery Period.
Average number of post-operative days with pain score >4/10. Pain score assessments were administered once daily by parents using either the Numeric Rating Scale (NRS-11) (with anchors 0=no pain and 10=highest pain imaginable) for children ages 8-15 (von Baeyer et al., 2009) or the Faces Pain Scale-Revised (FPS-R) (with anchors 0=no pain and 10=highest pain imaginable) for children ages 4-10 (Hicks et al., 2001).

Secondary Outcome Measures

Number of Participants Reporting Side Effects During the Post-tonsillectomy Recovery Period.
Parent-reported side effects entered in 10-day diary.

Full Information

First Posted
December 23, 2010
Last Updated
March 11, 2014
Sponsor
Children's Hospitals and Clinics of Minnesota
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1. Study Identification

Unique Protocol Identification Number
NCT01267136
Brief Title
A Comparison of Postoperative Tramadol Versus Acetaminophen With Codeine in Children Undergoing Tonsillectomy
Official Title
A Comparison of Postoperative Tramadol Versus Acetaminophen With Codeine in Children Undergoing Tonsillectomy
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
May 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospitals and Clinics of Minnesota

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Tonsillectomy is the most common pediatric surgical procedure performed in the US. The postoperative period can be particularly painful. Codeine (usually in mixed formulation with acetaminophen) is the most commonly prescribed opioid in the US. However, evolving data questions its ability to provide optimal pain relief, while avoiding side effects, especially in the postoperative setting. Tramadol may be a better option for children in the postoperative setting due to its well-documented analgesic properties, low potential for side effects, and excellent safety profile. Seventy-two children scheduled to undergo tonsillectomy (with or without adenoidectomy) at Children's will be invited to participate in a randomized, prospective, double-blinded study to evaluate the efficacy and side effects of codeine with acetaminophen versus tramadol. Using a 10-day take-home diary, caregivers will be asked to record daily information about their child's postoperative pain and other core outcomes and domains as recommended in the recent consensus statement put forth by the Pediatric Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials (IMMPACT) (McGrath et al., 2008). This study will offer new information regarding the efficacy and side effects associated with tramadol as compared with codeine/acetaminophen (the current practice standard) in a pediatric population. Hypotheses H1: Children who receive scheduled tramadol following tonsillectomy will report better pain control than children who receive scheduled codeine/acetaminophen. H2: Children who receive scheduled tramadol following tonsillectomy will report fewer side effects than children who receive scheduled codeine/acetaminophen.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tonsillitis, Pain
Keywords
Tonsillectomy, Pain, Pediatric, Opioids, Tramadol, Codeine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
84 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Capital® with Codeine Suspension
Arm Type
Experimental
Arm Title
Tramadol suspension
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Codeine with acetaminophen
Other Intervention Name(s)
Capital® with Codeine Suspension, Acetaminophen and Codeine phosphate suspension
Intervention Description
Liquid codeine/acetaminophen (Capital® 5mL= 120mg acetaminophen/12 mg codeine) 0.72 mg/kg [=0.3 mL/kg] (max. 36 mg) PO Q6h, plus 0.72 mg/kg (max. 36 mg) PO Q3h pro re nata (PRN) (max. of 3 PRN doses/day)
Intervention Type
Drug
Intervention Name(s)
Tramadol suspension
Other Intervention Name(s)
tramadol hydrochloride, Ultram
Intervention Description
Liquid tramadol 1.05 mg/kg [=0.3 mL/kg] (max. 52.5 mg) PO Q6h, plus 1.05 mg/kg (max. 52.5 mg) PO Q3h PRN (max. of 3 PRN doses/day).
Primary Outcome Measure Information:
Title
Efficacy of Two Different Liquid Pain Medications: Tramadol vs. Codeine/Acetaminophen During the Post-tonsillectomy Recovery Period.
Description
Average number of post-operative days with pain score >4/10. Pain score assessments were administered once daily by parents using either the Numeric Rating Scale (NRS-11) (with anchors 0=no pain and 10=highest pain imaginable) for children ages 8-15 (von Baeyer et al., 2009) or the Faces Pain Scale-Revised (FPS-R) (with anchors 0=no pain and 10=highest pain imaginable) for children ages 4-10 (Hicks et al., 2001).
Time Frame
Efficacy was assessed daily during the 10-day postoperative recovery period.
Secondary Outcome Measure Information:
Title
Number of Participants Reporting Side Effects During the Post-tonsillectomy Recovery Period.
Description
Parent-reported side effects entered in 10-day diary.
Time Frame
Side effects will be observed and recorded daily by caregivers for a total of 10 days in the take-home diary.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Child must be scheduled to undergo tonsillectomy (with or without adenoidectomy). Child must be between the ages of 4 and 15 at the time of enrollment. Child and caregiver must be English-speaking. The same caregiver (e.g., mother) must agree to complete all study assessments with child to ensure consistency. Exclusion Criteria: Child cannot self-assess pain due to conditions such as developmental delays, chromosomal abnormalities, and other syndromes. Child had significant adverse effects to codeine, tramadol, or acetaminophen in the past. Child has a known underlying seizure disorder (not febrile seizure). Child has known underlying renal or liver dysfunction (with creatinine, aspartate aminotransferase [AST]/amino alanine transferase [ALT], above normal value for age, respectively). Child or caregiver is not English-speaking. The same caregiver (e.g., mother) is unable to complete all follow-up assessments.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefan J Friedrichsdorf, M.D.
Organizational Affiliation
Children's Hospitals and Clinics of Minnesota
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospitals and Clinics of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55404
Country
United States

12. IPD Sharing Statement

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A Comparison of Postoperative Tramadol Versus Acetaminophen With Codeine in Children Undergoing Tonsillectomy

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