Status:
COMPLETED
Perioperative Analgesia in Neonates Who Underwent Primary Cleft Lip Repair Surgery
Lead Sponsor:
Brno University Hospital
Collaborating Sponsors:
Masaryk University
Conditions:
Perioperative Analgesia in Neonates
Eligibility:
All Genders
Up to 28 years
Brief Summary
In retrospective data search the investigators will identified the cumulative consumption of opioid analgesics during surgery and 24 hours after surgery in neonate with cleft lips who underwent primar...
Detailed Description
The cumulative consumption of opioids during surgery and 24 hours after surgery in neonates with cleft lips who underwent primary cleft lip repair surgery is not known. Patients were divided into two ...
Eligibility Criteria
Inclusion
- neonates with unilateral or bilateral cleft lip (U/BCL), all neonates with unilateral or bilateral cleft lip and alveolus (U/BCLA) or with unilateral or bilateral cleft lip, alveolus and palate (total cleft; U/BCLAP) who underwent cleft lip repair surgery in the neonatal period
- the study period (1/2018-12/2021)
Exclusion
- ● presence of coagulopathy
- thrombocytopenia or thrombopathy
- patients at risk of malignant hyperthermia
- patients who were not neonates (older than 28 days)
- patients who required postoperative mechanical ventilation
Key Trial Info
Start Date :
January 1 2018
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 1 2022
Estimated Enrollment :
111 Patients enrolled
Trial Details
Trial ID
NCT06067854
Start Date
January 1 2018
End Date
January 1 2022
Last Update
September 8 2025
Active Locations (1)
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1
Brno University Hospital
Brno, South Moravian, Czechia, 62500