- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06396000
Factors Analysis Related to Prolonged Stay in the Pediatric Post-Anesthesia Care Unit(PACU) (PACU)
Prolonged Stay in the Pediatric PACU
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Estimated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Children aged 0-18 years old; Child entering the Pediatric Post-Anesthesia Care.
- Emergency surgery; Pediatric patients with incomplete medical history; Pediatric patients requiring postoperative ICU care; Pediatric patients with preoperative altered consciousness; Neurological disorders; Severe liver, kidney, lung, and heart diseases.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anesthesia Plan Selection
Time Frame: Day 1
|
Anesthesia options include general anesthesia, combined anesthesia, pure intravenous anesthesia, and nerve block anesthesia.
|
Day 1
|
|
Pain Score
Time Frame: Day 1
|
Evaluate pain using the Visual Analog Scale (VAS): 0 points: no pain; 1-3 points: mild pain; 4-6 points: moderate pain; 7-10 points: severe pain.
|
Day 1
|
|
Complications in PACU
Time Frame: Day 1
|
Nausea, vomiting, chills, pain, agitation
|
Day 1
|
|
American Society of Anesthesiologists(ASA)
Time Frame: Day 1
|
ASA I: Patients in good health, without systemic disease. ASA II: Patients with mild systemic disease, not significantly limiting daily activity. ASA III: Patients with severe systemic disease, with definite functional limitation. ASA IV: Patients with severe systemic disease that is a constant threat to life. ASA V: Moribund patients who are not expected to survive without the operation. ASA VI: Brain-dead patients whose organs are being removed for donation. |
Day 1
|
|
The medication usage in PACU
Time Frame: Day 1
|
Morphine, Propofol, Ketorolac, Fentanyl
|
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The use of PCA(Patient-Controlled Analgesia)in PACU
Time Frame: Day 1
|
PCA usage statistics,yes or no
|
Day 1
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- FARPSPP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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