- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT02202174
The Safety and Efficacy of Supraglottic Airway Use in Children
연구 개요
상세 설명
This study aims to understand the efficacy of supraglottic airway (SGA) use in children in a tertiary care Children's Hospital.
Observational data regarding the type of SGA, experience level of practitioner, placement technique, number of placement attempts or placement failure, device failure, and cause of any related peri-operative complications will be prospectively collected.
The data collected in this study will allow the investigators to assess the overall safety and efficacy of SGA use in various medical and surgical procedures performed under general anesthesia in children.
연구 유형
등록 (예상)
연락처 및 위치
연구 장소
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Illinois
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Chicago, Illinois, 미국, 60611
- 모병
- Ann & Robert H. Lurie Children's Hospital of Chicago
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연락하다:
- Narasimhan Jagannathan, MD
- 이메일: simjag2000@yahoo.com
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수석 연구원:
- Narasimhan Jagannathan, MD
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
설명
Inclusion Criteria:
- Children undergoing anesthesia with use of a supraglottic airway device as a primary means of oxygenation & ventilation
Exclusion Criteria:
- N/A
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
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Supraglottic Airway Device
Patients will receive a supraglottic airway device as a primary means of ventilation.
The following devices may be used: LMA Unique, LMA ProSeal, LMA Supreme, LMA Flexible, Ambu Aura-I, Ambu Aura Once, Air-Q, I-Gel, or other supraglottic airway device.
Choice of the device will be clinician dependent and based on the patients body weight per manufacturer guidelines
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다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
Supraglottic Airway Device Failure
기간: participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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Occurrence and reason for supraglottic airway device failure (ie inadequate ventilation, laryngospasm, bronchospasm, etc) will be recorded in addition to conversion to tracheal intubation
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participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
Ease of Placement of Supraglottic Airway Device
기간: participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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Ease of placement of supraglottic airway device ranging from 1 (easy) to 4 (difficult)
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participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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Multiple Attempts to Place Supraglottic Airway Device
기간: participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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change in device, placement method, and provider will be recorded
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participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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Airway Maneuvers/interventions
기간: participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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the number and type of airway maneuvers performed after device placement and during maintenance will be recorded
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participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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Occurrence of Inadequate Ventilation
기간: participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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cause and solution for inadequate ventilation will be recorded
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participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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Intraoperative Complications
기간: participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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Time period of complication (ie during device placement, maintenance, or removal) and cause of complication (ie.
dental injury, light anesthesia, regurgitation, laryngospasm, bronchospasm, aspiration, etc.) will be recorded
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participants will be followed for the duration of anesthesia and after surgery, an expected average of 12 hours
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Postoperative Complications
기간: participants will be followed for the duration of anesthesia and 24 hours postoperatively
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Complications noted postoperatively relating to reflex activation of the airway, sore throat, or hoarseness
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participants will be followed for the duration of anesthesia and 24 hours postoperatively
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공동 작업자 및 조사자
수사관
- 수석 연구원: Narasimhan Jagannathan, MD, Ann & Robert H. Lurie Children's Hospital of Chicago / Stanley Manne Research Institute
간행물 및 유용한 링크
일반 간행물
- Lopez-Gil M, Brimacombe J, Alvarez M. Safety and efficacy of the laryngeal mask airway. A prospective survey of 1400 children. Anaesthesia. 1996 Oct;51(10):969-72. doi: 10.1111/j.1365-2044.1996.tb14968.x.
- Mathis MR, Haydar B, Taylor EL, Morris M, Malviya SV, Christensen RE, Ramachandran SK, Kheterpal S. Failure of the Laryngeal Mask Airway Unique and Classic in the pediatric surgical patient: a study of clinical predictors and outcomes. Anesthesiology. 2013 Dec;119(6):1284-95. doi: 10.1097/ALN.0000000000000015.
- Jagannathan N, Sequera-Ramos L, Sohn L, Wallis B, Shertzer A, Schaldenbrand K. Elective use of supraglottic airway devices for primary airway management in children with difficult airways. Br J Anaesth. 2014 Apr;112(4):742-8. doi: 10.1093/bja/aet411. Epub 2013 Dec 8.
- Asai T. Is it safe to use supraglottic airway in children with difficult airways? Br J Anaesth. 2014 Apr;112(4):620-2. doi: 10.1093/bja/aeu005. Epub 2014 Feb 20. No abstract available.
- Bordet F, Allaouchiche B, Lansiaux S, Combet S, Pouyau A, Taylor P, Bonnard C, Chassard D. Risk factors for airway complications during general anaesthesia in paediatric patients. Paediatr Anaesth. 2002 Nov;12(9):762-9. doi: 10.1046/j.1460-9592.2002.00987.x.
- Lalwani K, Richins S, Aliason I, Milczuk H, Fu R. The laryngeal mask airway for pediatric adenotonsillectomy: predictors of failure and complications. Int J Pediatr Otorhinolaryngol. 2013 Jan;77(1):25-8. doi: 10.1016/j.ijporl.2012.09.021. Epub 2012 Oct 11.
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (예상)
연구 완료 (예상)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
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