- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01866501
혼합 기술을 검증하는 후속 연구
근위 상완골 골내 혈관 접근 삽입 부위를 식별하기 위한 혼합 기법의 검증을 위한 후속 연구
연구 개요
상세 설명
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Texas
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Spring Branch, Texas, 미국, 78070
- Bulverde-Spring Branch EMS
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
설명
포함 기준:
- 현재 면허가 있거나 인증된 응급 의학 기사, 구급대원 또는 간호사 근위 상완골 IO 삽입 부위 사용에 대한 정식 교육을 받은 적이 없습니다. 교육 부분 동안 장치 및 기술의 적절한 사용을 시연하고 장치 트레이너로부터 참여 승인을 얻습니다.
제외 기준:
- 근위 상완골 골내 혈관 접근 확립에 대한 이전 교육
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 다른
- 할당: 무작위화되지 않음
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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다른: Blended Technique for Intraosseous Insertion
Clinician device operators will be trained on the Blended Technique site identification method and perform one unilateral proximal humerus (PH) intraosseous needle insertion.
The blended technique is: The arm is positioned with the elbow adducted and shoulder internally rotated with the hand over the abdomen.
The operator places one hand in the axilla and the other hand along the midline of the upper arm laterally, to define the anterior and posterior borders.
The vertical plane of insertion lies in the middle of these borders.
Along the vertical axis, deeply palpate the PH until the junction of the surgical neck and humeral head is identified.
The insertion site is the greater tubercle, about 1-2 cm superior to the surgical neck.
Secondary confirmation is made by palpating the inter-tubercular groove with a 90º rotation of the arm, confirming the insertion site is lateral to the groove, and returning the arm back to a medially rotated position with the hand over the abdomen
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Intraossesous Vascular Access in the proximal humerus
다른 이름들:
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다른: Healthy Subjects: Blended Technique
Healthy subjects will receive bilateral intraosseous vascular access established in the proximal humerus performed by device operators using the blended technique.
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Intraossesous Vascular Access in the proximal humerus
다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Proximal Humerus Intraosseous (IO) Insertion Site Placement Total Score
기간: Day 1 Within 10 minutes following procedure
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X-ray images of the inserted IO needle will be used to evaluate placement success and scored. Each insertion is scored by a musculoskeletal radiologist for two measures: Insertion Site Accuracy (scale range 0 - 3) and Needle Tip Location (scale range -7 to 7) as described below. The Total score is the sum of Insertion Site Accuracy Score and Needle Tip Location Score. Scale range -7 to 10; higher score indicates greater accuracy. Insertion Site Accuracy Score Scale is 0 to 3 where higher scores indicate greater accuracy: 3=center of greater tubercle, 2=perimeter of greater tubercle, 1=junction of greater tubercle and shaft or head, and 0=outside the greater tubercle. Needle tip Location Score Scale ranges from -7 to 7 where higher scores indicate more favorable needle tip location: 7=within center of proximal humerus (PH), 5=within PH not centered, 3= Near miss of PH, -3=In humeral head, -3=on epiphyseal line, -5=lateral miss (of the humerus), -7=medial miss (of the humerus). |
Day 1 Within 10 minutes following procedure
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Time to Intraosseous Catheter Placement
기간: 1 day, within 10 minutes of procedure
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The amount of time it takes for the device operator to identify the proximal humerus intraosseous (IO) insertion site using their assigned proximal humerus IO site identification method and insert the IO needle.
Timing starts from the time the participant begins to palpate the proximal humerus and stops when the IO needle is inserted.
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1 day, within 10 minutes of procedure
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Level of Confidence Score Pre-intraosseous Insertion
기간: Day 1 within 10 minutes of completing training
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Device operators scored their perceived Level of Confidence with their assigned Intraosseous (IO) Insertion method.
The score was reported following the completion of training but before performing the unilateral IO insertion.
The Level of Confidence scale scores range from 1 to 5, where.
1=not at all confident, 2=slightly confident, 3=moderately confident, 4=very confident, and 5=extremely confident.
Higher scores indicate greater level of confidence.
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Day 1 within 10 minutes of completing training
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Level of Confidence Score Post-intraosseous Insertion
기간: Day 1 within 10 minutes of completing the unilateral intraosseous insertion
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Device operators scored their perceived Level of Confidence with their assigned Intraosseous (IO) Insertion method for their one unilateral proximal humerus IO site procedure.
The score was reported after performing the unilateral IO insertion.
The Level of Confidence scale scores range from 1 to 5, where.
1=not at all confident, 2=slightly confident, 3=moderately confident, 4=very confident, and 5=extremely confident.
Higher scores indicate greater level of confidence.
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Day 1 within 10 minutes of completing the unilateral intraosseous insertion
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Ease of Use Score Pre-intraosseous Insertion
기간: Day 1 within 10 minutes of completing the unilateral intraosseous insertion
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Device operators will score their perceived Ease of Use for their assigned Intraosseous Insertion method for their one unilateral proximal humerus IO site procedure.
The score was reported following the completion of training but before performing the unilateral IO insertion.
The Ease of Use scale scores range from 1 to 5, where 1=very difficult, 2=difficult, 3=neutral, 4=easy, and 5=very easy.
Higher scores indicate greater ease of use.
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Day 1 within 10 minutes of completing the unilateral intraosseous insertion
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Ease of Use Score Post-intraosseous Insertion
기간: Day 1 within 10 minutes of completing the unilateral insertion
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Device operators will score their perceived Ease of Use for their assigned Intraosseous Insertion method for their one unilateral proximal humerus IO site procedure.
The score was reported after completing the unilateral intraosseous insertion.
The Ease of Use scale scores range from 1 to 5, where 1=very difficult, 2=difficult, 3=neutral, 4=easy, and 5=very easy.
Higher scores indicate greater ease of use.
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Day 1 within 10 minutes of completing the unilateral insertion
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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Intraosseous Infusion Flow Rates
기간: Day 1 after establishing IO vascular access
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Intraosseous infusion flow rates attained at tested infusion pressures, which may include Gravity; 100 mmHg, 200 mmHg and 300 mmHg.
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Day 1 after establishing IO vascular access
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Time in Seconds for Fluid Delivery From the Proximal Humerus to the Heart
기간: Day 1 after IO insertion
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Time in seconds for fluid delivery from the proximal humerus to the heart, using visualization of contrast injection under fluoroscopy was performed and measured once for the participants in the Healthy Subjects: Blended Technique arm.
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Day 1 after IO insertion
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Success Rate of Obtaining Laboratory Results for Both Intraosseous and Peripheral Venous Specimens
기간: Day 1 within 30 minutes after establishing proximal humerus IO vascular access and peripheral venous access
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Number of Participants with Laboratory Results Successfully Obtained from both intraosseous (IO) and peripheral venous blood specimens.
Success was determined if the point-of-care laboratory analysis system provided laboratory results values for both IO and Peripheral Venous specimens.
It was deemed unsuccessful if the point-of-care system provided no laboratory results values and/or noted an error for at least one specimen.
An intraosseous blood specimen and a peripheral venous blood specimen were collected from each subject
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Day 1 within 30 minutes after establishing proximal humerus IO vascular access and peripheral venous access
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공동 작업자 및 조사자
수사관
- 수석 연구원: Larry J Miller, MD, Vidacare Corporation
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정된)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .