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NCT Number: NCT02361476

Does Intraoperative Clonidine Reduce Post Operative Agitation in Children?

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.

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Key information

Age range

1 year–5 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

The Juliane Marie Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Region Sjælland, Denmark

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Clonidine

Drug

Injection - during surgery

Other names: catapresan

Placebo

Drug

Injection - during surgery

Other names: NaCl

Primary outcomes

  1. Postoperative Agitation

    Time frame: 1 day

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

Secondary outcomes

  1. Fentanyl and Morphine Requirements

    Time frame: Recorded during the stay in the postoperative recovery room

    Amount used

  2. Pain Assessment

    Time frame: recovery room - hours

    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

  3. First Administration of Fentanyl or Morphine

    Time frame: recovery room

    Time to administration

  4. Adverse Events

    Time frame: from intervention to discharge from the recovery room

Sponsors and collaborators

Lead sponsor

Rigshospitalet, Denmark

Other

Registry information

Official study title

Does Intraoperative Clonidine Reduce Post Operative Agitation in Children Anaesthetised With Sevoflurane? A RCT Including Pharmacokinetic Investigation.

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Feb 11, 2015
Registry last updated
Feb 11, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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