search
Back to results

Does Intraoperative Clonidine Reduce Post Operative Agitation in Children?

Primary Purpose

Psychomotor Agitation

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Clonidine
Placebo
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Psychomotor Agitation focused on measuring Anaesthesia, Children, Clonidine, Sevoflurane, Postoperative agitation, Prevention, Pharmacokinetics, Safety

Eligibility Criteria

1 Year - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • scheduled for surgery with Sevoflurane as the choice of anesthesia.

Exclusion Criteria:

  • ASA classification >2
  • Premedication with Clonidine
  • Ex-premature (born before week 37+0 AND <60 weeks old)
  • Intubated before anaesthesia and/or no plans for extubation after anaesthesia.
  • Critical illness with haemodynamic instability.
  • Active bleeding.
  • Cancer.
  • Cardiac diseases including arrhythmias.
  • Malignant hyperthermia.
  • Mental retardation.
  • Neurological illness with agitation-like symptoms.
  • Weight >50 kg.
  • Allergy to Clonidine.
  • Patients treated with methylphenidate / Concerta.

Sites / Locations

  • The Juliane Marie Centre, Copenhagen University Hospital, Rigshospitalet
  • Køge Sygehus, Anæstesiologisk Afdeling
  • Anæstesiologisk afdeling, Vejle Sygehus

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Intervention

Placebo

Arm Description

Clonidine : injection og 3 micg/kg IV during the operation.

Placebo : injection og equal amount of NaCl IV during the operation.

Outcomes

Primary Outcome Measures

Postoperative Agitation
Measured by Watchae Scale (score 1-4), scores 1-2 = no agitation and scores 3-4 = agitated

Secondary Outcome Measures

Fentanyl and Morphine Requirements
Amount used
Pain Assessment
Pain score used: FLACC score = Face, Legs, Activity, Cry, Consolability Score ranges from 0 to 10 (severity increases with increasing score) Pain is FLACC score more than 3
First Administration of Fentanyl or Morphine
Time to administration
Adverse Events

Full Information

First Posted
February 1, 2015
Last Updated
September 11, 2018
Sponsor
Rigshospitalet, Denmark
search

1. Study Identification

Unique Protocol Identification Number
NCT02361476
Brief Title
Does Intraoperative Clonidine Reduce Post Operative Agitation in Children?
Official Title
Does Intraoperative Clonidine Reduce Post Operative Agitation in Children Anaesthetised With Sevoflurane? A RCT Including Pharmacokinetic Investigation.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Clonidine is widely used off-label in children for several indications. Clonidine is used for treatment and/or prevention of postoperative agitation in children anaesthetised with Sevoflurane. The investigators don´t have solid evidence for the effect and the investigators don´t have data for characterization of the pharmacokinetic profile among age-groups for children 1-6 years. In this study the investigators want to investigate if IV Clonidine administered at the end of surgery can prevent/reduce postoperative agitation. Secondary outcomes include measurements of postoperative pain relief and adverse effects, including a 30-day follow-up.
Detailed Description
BACKGROUND: Clonidine is widely used off-label in children for several indications such as treatment and/or prevention of postoperative agitation when anaesthetised with Sevoflurane. However, the current level of evidence in support of Clonidine treatment for postoperative agitation in children remains limited. In addition, the pharmacokinetic profile of intravenous Clonidine in children is not well characterized for age-groups. METHODS/DESIGN: In this prospective multicentre double-blinded randomized clinical trial, the investigators aim to investigate the impact of intravenous (IV) Clonidine administered at the end of surgery, on the incidence and degree of postoperative agitation. Children will be assigned to either the intervention or the placebo group. The allocation will be carried out centrally and stratified based on age and trial-site, with152 patients allocated to each group. In the intervention group, 3 micrograms per kg of IV clonidine is administered approximately 20 minutes before the expected completion of the surgery (as assessed by the surgeon). In the control group; Saline (placebo) is injected in equal quantity during surgery at the same time. The drugs are concealed in identical blinded ampoules. The primary outcome is postoperative agitation measured on the Watcha scale. Secondary outcomes include measurements of postoperative pain relief and adverse effects, including 30-day follow-up. Twenty of the patients age 1-2 years and twenty age >2 years, with a peripheral venous access in place, will be allocated to drug assay sampling; enabling a compartmental PK analysis based on age group, using non-linear mixed effects models.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychomotor Agitation
Keywords
Anaesthesia, Children, Clonidine, Sevoflurane, Postoperative agitation, Prevention, Pharmacokinetics, Safety

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Clonidine : injection og 3 micg/kg IV during the operation.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo : injection og equal amount of NaCl IV during the operation.
Intervention Type
Drug
Intervention Name(s)
Clonidine
Other Intervention Name(s)
catapresan
Intervention Description
Injection - during surgery
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
NaCl
Intervention Description
Injection - during surgery
Primary Outcome Measure Information:
Title
Postoperative Agitation
Description
Measured by Watchae Scale (score 1-4), scores 1-2 = no agitation and scores 3-4 = agitated
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Fentanyl and Morphine Requirements
Description
Amount used
Time Frame
Recorded during the stay in the postoperative recovery room
Title
Pain Assessment
Description
Pain score used: FLACC score = Face, Legs, Activity, Cry, Consolability Score ranges from 0 to 10 (severity increases with increasing score) Pain is FLACC score more than 3
Time Frame
recovery room - hours
Title
First Administration of Fentanyl or Morphine
Description
Time to administration
Time Frame
recovery room
Title
Adverse Events
Time Frame
from intervention to discharge from the recovery room

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: scheduled for surgery with Sevoflurane as the choice of anesthesia. Exclusion Criteria: ASA classification >2 Premedication with Clonidine Ex-premature (born before week 37+0 AND <60 weeks old) Intubated before anaesthesia and/or no plans for extubation after anaesthesia. Critical illness with haemodynamic instability. Active bleeding. Cancer. Cardiac diseases including arrhythmias. Malignant hyperthermia. Mental retardation. Neurological illness with agitation-like symptoms. Weight >50 kg. Allergy to Clonidine. Patients treated with methylphenidate / Concerta.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steen Henneberg, MD, DMSc
Organizational Affiliation
Rigshospitalet, Denmark
Official's Role
Study Director
Facility Information:
Facility Name
The Juliane Marie Centre, Copenhagen University Hospital, Rigshospitalet
City
Copenhagen
State/Province
Zealand
ZIP/Postal Code
2100
Country
Denmark
Facility Name
Køge Sygehus, Anæstesiologisk Afdeling
City
Køge
ZIP/Postal Code
4600
Country
Denmark
Facility Name
Anæstesiologisk afdeling, Vejle Sygehus
City
Vejle
ZIP/Postal Code
7100
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
24727829
Citation
Pickard A, Davies P, Birnie K, Beringer R. Systematic review and meta-analysis of the effect of intraoperative alpha(2)-adrenergic agonists on postoperative behaviour in children. Br J Anaesth. 2014 Jun;112(6):982-90. doi: 10.1093/bja/aeu093. Epub 2014 Apr 11.
Results Reference
background
PubMed Identifier
30169192
Citation
Ydemann M, Nielsen BN, Henneberg S, Jakobsen JC, Wetterslev J, Lauritsen T, Steen N, Edstrom B, Afshari A; PREVENT AGITATION Research Group. Intraoperative clonidine for prevention of postoperative agitation in children anaesthetised with sevoflurane (PREVENT AGITATION): a randomised, placebo-controlled, double-blind trial. Lancet Child Adolesc Health. 2018 Jan;2(1):15-24. doi: 10.1016/S2352-4642(17)30127-X. Epub 2017 Nov 2.
Results Reference
derived
PubMed Identifier
27264945
Citation
Ydemann M, Nielsen BN, Wetterslev J, Henneberg S, Lauritsen T, Steen N, Edstrom B, Afshari A. Effect of clonidine to prevent agitation in children after sevoflurane anaesthesia: a randomised placebo controlled multicentre trial. Dan Med J. 2016 Jun;63(6):A5234.
Results Reference
derived

Learn more about this trial

Does Intraoperative Clonidine Reduce Post Operative Agitation in Children?

We'll reach out to this number within 24 hrs