- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01479673
TICACOS International (P2 -RMCS)
Tight Caloric Balance in ICU Patients: a Multicenter, Prospective, Randomized, Controlled Study.
The aim of this study is to perform a prospective, randomized, controlled blinded study in critically patients to assess the necessity for measuring daily resting energy expenditure as a guide for nutritional support. Our hypothesis is that tight caloric control will reduce the rate of new infections.
Study Design :Multi-center, randomized, single blinded, controlled study. Study Population: newly-admitted, adult mechanically ventilated ICU patients.
연구 개요
상태
정황
상세 설명
Study objectives
To evaluate the effect of tight caloric control in critical patients on:
- The rate of acquired nosocomial infections (Ventilated associated pneumonia, Catheter related infections, Urinary tract infections)
- Mortality rates, length of stay in the ICU and in hospital, length of ventilation and incidence of non-infectious complications.
Primary endpoint:
Rate of nosocomial infections (for definitions see appendage 1) acquired after 48 to 72 hours following admission.
Secondary endpoints
- Metabolic control: glucose concentration, insulin administration, rate of hypoglycemic events.
- Success of tight caloric control: accumulative and maximum negative energy balance.
- Organ function: SOFA score.
- Rate of non-infectious complications: requirement for surgery or occurrence of pressure sores.
- Length of ICU stay and of assisted ventilation (LOS and LOV)
- ICU survival rate.
- Patient status and disposition on day 28 or at hospital discharge.
- 3 & 6 months survival.
연구 유형
등록 (예상)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Petach Tikva, 이스라엘, 49100
- 모병
- Rabin Medical Center, Campus Beilinson
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연락하다:
- Pierre Singer, Professor,MD
- 전화번호: 972-39376521
- 이메일: psinger@clalit.org.il
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부수사관:
- Ronit Anbar, RD
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연락하다:
- Milana Grinev, Study Coordinator
- 전화번호: 972-39376590
- 이메일: milang@clalit.org.il
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Mechanically-ventilated adults(Male or Female)admitted to general ICU within the first 48 hours of ICU admission.
- Age ≥ 18 years;no upper age limit.
- Expected stay in ICU> 3 days: [SAPS II (18) > ICU median or high-level of nursing care implemented or per clinical impression of attending physician]
- Medical and abdomino/thoracic surgery patients, as well as multiple trauma patients with Glasgow Coma Score ≥ 10.
Exclusion Criteria:
- Pregnancy.
- DNR order.
- Readmission in the ICU during the same hospitalization/transfer from other ICU.
- Admission for postoperative monitoring.
- Respiratory instability: SpO2 <90% or need for ventilator adjustments during the preceding hour or hyperventilation (Respiratory rate > 35/min)
- Bicarbonate infusion, loss of bicarbonate (diarrhea, ureterosogmoidostomy or use of acetazoloamide, ultrafiltration).
- Aerosolization with nitric oxide or heliox, tracheal insufflations or visible leaks in chest drainage system.
- FiO2 80% or patients requiring prone position
- Chronic/acute liver failure:Child-Pugh class C
- Brain injury for various reasons with Glasgow Coma Scale below 10.
- Cardiac surgery patients.
- Patients in the hospital for more than 7 days.
- Contra indication to use enteral nutrition.
- Participation in a clinical study with an investigational drug within one month prior to the start of this clinical trial.
- Ethical issues that will influence subject eligibility.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 특수 증상
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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간섭 없음: Control group
Patients in this group will receive enteral nutrition/parenteral nutrition or combination of enteral and parenteral nutrition according to the "liberal " regimen, i.e. according to local practice.
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실험적: Indirect Calorimetry
Study group: Indirect Calorimetry (IC) Patients in this group will receive enteral nutrition/parenteral nutrition or combination of enteral and parenteral nutrition according to the individual energy requirements calculated by Indirect Calorimetry measurement of Resting Energy Expenditure (REE).
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Patients in this group will receive enteral nutrition/parenteral nutrition or combination of enteral and parenteral nutrition according to the individual energy requirements calculated by Indirect Calorimetry.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Rate of nosocomial infections
기간: After 48 to 72 hours /daily assessment: within 28 day
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Rate of nosocomial infections acquired after 48 to 72 hours following admission up to day 28/or discharge will be evaluated
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After 48 to 72 hours /daily assessment: within 28 day
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Metabolic control
기간: Day 1 up to day 28/or discharge
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Glucose concentration, insulin administration, rate of hypoglycemic events will be daily assessed
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Day 1 up to day 28/or discharge
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Caloric control
기간: Day 1 up to day 28/or discharge
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Success of tight caloric control:accumulative and maximum negative energy balance
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Day 1 up to day 28/or discharge
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공동 작업자 및 조사자
수사관
- 수석 연구원: Pierre Singer, MD, Professor, RabinMC,Beilinson Hospital
- 연구 책임자: Milana Grinev, RN,Study Coordinator, RabinMC, Beilinson Hospital ,Petah- Tikva, Israel
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
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. .
기계적 환기 합병증에 대한 임상 시험
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Ruijin Hospital완전한심각한 병 | 호흡 부전 | 폐관류 | Ventilation-Perfusion Ratio중국