1=The inner and outer canthus line across the central cornea; 2= Inferior limbus does not exceed the inner and outer canthus line; 3= Inferior limbus exceed the inner and outer canthus line.
Comparison of Sedation by Esketamine and Sevoflurane
Brief Summary
Intervention / Treatment
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Sevoflurane (DRUG)All patients received 0.01 mg/kg atropine and 1ug/kg dexmedetomidine iv as premedication.5% sevoflurane(FIO2=100%, 3L·min-1) was used to induce anaesthesia by mask inhalation and 3-4 % sevoflurane (adjusted according to the depth of the anaesthesia,FIO2=100%, 2L·min-1) was maintained
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Esketamine (DRUG)All patients received 0.1 mg/kg atropine and 1ug/kg dexmedetomidine iv as premedication.0.5mg·kg-1 esketamine was administered by vein in one minute, and 0.25mg·kg-1 esketamine was given at the beginning of the surgery.
Condition or Disease
- Sevoflurane
Phase
Study Design
Study type: | INTERVENTIONAL |
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Status: | Unknown status |
Study results: | No Results Available |
Age: | 3 Months to 6 Years |
Enrollment: | 60 (ESTIMATED) |
Allocation: | Randomized |
Primary Purpose: | Supportive Care |
MaskingTRIPLE:
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Clinical Trial Dates
Start date: | Sep 20, 2021 | ACTUAL |
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Primary Completion: | Dec 31, 2021 | ACTUAL |
Completion Date: | Apr 20, 2022 | ESTIMATED |
Study First Posted: | Aug 18, 2021 | ACTUAL |
Last Updated: | Mar 25, 2022 |
Sponsors / Collaborators
Ketamine is widely used for procedural sedation, which produces a dissociated state with minimal risk of airway compromise or apnea. Esketamine is the S (+) isomer of ketamine, It has enhanced analgesic potency and faster elimination compared to ketamine. However, it may also cause agitation during the recovery time. Based on these experiences on ketamine, we compared the effectiveness of esketamine and sevoflurane for short ophthalmological procedure in pediatric patients.
Participant Groups
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patients were anesthetized by face mask with 5 vol% sevoflurane with total 5 L/min-1 fresh gas flow. Anaesthesia was maintained by continuously using 3-4% sevoflurane.
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patients received 0.5mg/kg IV esketamine at first, after surgical field disinfection, another 0.25mg/kg IV esketamine was administered. Then 1mg/kg propofol was administered every 5 minutes after intubation.
Eligibility Criteria
Sex: | All |
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Maximum Age: | 6 |
Age Groups: | Child |
Healthy Volunteers: | Yes |
* patient who needed suture removal and ophthalmic examination
Exclusion Criteria:
* previous coronary heart disease,hypertension, arterial aneurysm, epilepsia, intracranial mass of benign or malign nature
Primary Outcomes
Secondary Outcomes
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decreased tidal volume or weak chest undulation
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the incidence of oxygen saturation below 95% caused by anesthetic agents
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Intraocular pressure after induction
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If the target level of sedation was not achieved, an additional 0.1mg/kg propofol was injected and repeated if necessary
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The Cole 5-point scale (CPS) score included five behaviors: 1=sleeping; 1=awake,calm;3=irritable, crying;4=inconsolable crying; 5=severe restlessness, disorientation.
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the time of the length of stay in the post-anesthesia care unit
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mean blood pressure
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Heart rate
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extubation time
More Details
NCT Number: | NCT05011214 |
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Other IDs: | esketamine |
Study URL: | https://clinicaltrials.gov/study/NCT05011214 |