KCT0001113Recruiting未知
Propofol-remifentanil or propofol-ketamine for burn care in pediatric patients
Bestian Medical Center0 sites70 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Recruiting
- Sponsor
- Enrollment
- 70
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional Study
Eligibility Criteria
- Ages
- o Limit to 10(Year) (—)
- Sex
- All
Inclusion Criteria
- •Patients scheduled for burn care under sedation are included.
Exclusion Criteria
- •Patients are excluded if they have a cardiovascular, cerebrovascular, pulmonary, renal or hepatic disease, or are at risk of aspiration.
Investigators
Similar Trials
Not yet recruiting
Not Applicable
Conscious sedation and vertebroplastyMusculoskeletal Diseasesconscious sedation ,vertebroplastyAnaesthesiaPACTR201801002914411Asmaa Fawzy Amer60
Recruiting
Phase 2
Comparative evaluation of two drug combinations of propofol-ketamine and propofol-fentanyl for total intravenous anaesthesia in short surgical proceduresCTRI/2019/06/019790Kalinga institute of medical sciences
Completed
Not Applicable
Suitability of propofol-remifentanil pharmacodynamic interaction modelgynecological diseaseJPRN-UMIN000028961Asahikawa Medical University100
Recruiting
Phase 4
Assessing the efficacy of Ketamine and Profopol mixed together in a single syringe to sedate or reduce pain during a procedure in the Emergency DepartmentCTRI/2017/10/010271Department of Emergency MedicineDepartment of Emergency Medicine Sri Ramachandra University
Completed
Not Applicable
Comparison of insertion conditions of a laryngeal mask airway under propofol-ketamine or propofol-fentanyl anesthesiaCTRI/2014/08/004905Institute120