Assessed via visual analog scale
Ketamine vs Propofol for Sedation During Pediatric Bronchoscopy
Brief Summary
Intervention / Treatment
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Ketamine (DRUG)N/A
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Propofol (DRUG)N/A
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midazolam and atropine (DRUG)N/A
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Lidocaine (DRUG)N/A
Condition or Disease
- Paediatric Flexible Bronchoscopy
Phase
Study Design
Study type: | INTERVENTIONAL |
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Status: | Suspended |
Study results: | No Results Available |
Age: | up to 18 Years (Child, Adult) |
Enrollment: | 150 (ESTIMATED) |
Funded by: | Other |
Allocation: | Randomized |
Primary Purpose: | Treatment |
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Clinical Trial Dates
Start date: | May 01, 2016 | |
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Primary Completion: | May 01, 2019 | ESTIMATED |
Completion Date: | May 01, 2019 | ESTIMATED |
Study First Posted: | Apr 19, 2016 | ESTIMATED |
Results First Posted: | Aug 31, 2020 | |
Last Updated: | Apr 27, 2017 |
Sponsors / Collaborators
Propofol is often used as the sedation drug for this procedure due to its rapid sedative effect and favorable emergence profile. Propofol's major limitation is its tendency to cause apneas, which can occur in a relatively narrow therapeutic window. Apnea risk decreases with the patient's age and administering physician's familiarity and experience with the drug.
Ketamine is a drug often used for pediatric procedural sedation. Its pharmacologic safety profile is very wide, allowing a wide spectrum of dosing with a significantly reduced risk of apnea when compared to propofol. Known adverse effects of the drug include its emergence profile which may be accompanied by hallucinations, bronchorrhea and laryngospasm. Hallucinations may be prevented by using benzodiazepines concurrently and are possibly more pronounced in teenaged children compared to infants, although post-sedation irritability in the latter group might be an expression of this. Bronchorrhea, while usually not of significant concern during procedural sedation, has the potential to play a more noteworthy role during bronchoscopy. Significant airway secretions can create a difficult working environment for the pulmonologist performing the procedure. Patient safety may also be affected, as increased airway secretions reduce visibility in pediatric airways that are narrow to begin with and further compromised by placement of the bronchoscope. Potentially, this might also impact on the child's air flow and gas exchange. Laryngospasm during the procedure potentially hinders passage of the scope beyond the vocal cords and might extend the duration of the procedure.
In the investigators' center, propofol has most often been the sedative drug of choice for bronchoscopy. Yet, ketamine has been used at times due to its safety profile and the administering physicians level of comfort with each drug.
Aim:
To compare operator satisfaction and adverse effects in children presenting for flexible bronchoscopy using ketamine versus propofol as the primary sedative agent.
Participant Groups
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All patients will be sedated according to a written protocol which includes intravenous administration of midazolam and atropine. In addition, local anesthesia will be performed using lidocaine 1% sprayed once just above the vocal cords, and again at the level of the carina. Lidocaine doses are limited to a maximum total dose of 5mg/kg. This study group will be exposed to ketamine as the main drug for sedation, as an initial bolus of 1-2 mg/kg initially and then titrated by additional doses of 1mg/kg per dose.
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All patients will be sedated according to a written protocol which includes intravenous administration of midazolam and atropine. In addition, local anesthesia will be performed using lidocaine 1% sprayed once just above the vocal cords, and again at the level of the carina. Lidocaine doses are limited to a maximum total dose of 5mg/kg. This study group will be exposed to propofol as the main drug for sedation, as an initial bolus of 1-2 mg/kg initially and then titrated by additional doses of 1mg/kg per dose.
Eligibility Criteria
Sex: | All |
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Maximum Age: | 18 |
Age Groups: | Child / Adult |
Healthy Volunteers: | Yes |
* Children undergoing flexible bronchoscopy
Exclusion Criteria:
* Failure to acquire parental consent
* Bronchoscopies performed outside of the bronchoscopy suite
* Bronchoscopies performed under general anesthesia with a protected airway
* Bronchoscopies performed by personnel outside of the study group
* Known allergies to either of the sedation drugs used
Primary Outcomes
Secondary Outcomes
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Assessed via visual analog scale
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Assessed via visual analog scale
More Details
NCT Number: | NCT02743104 |
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Other IDs: | KP-001 |
Study URL: | https://clinicaltrials.gov/study/NCT02743104 |