DEVICE
protective ventilation
Patients with moderate to severe ARDS received ventilation treatment according to predicted body weight(PBW) and controlled plateau pressure.
Status
Unknown
Phase
Phase 4
Enrollment
1,000
Locations
11
Results
Not posted
Publications
12
Study summary
Platform adaptive embedded trial for acute respiratory distress syndrome (PETARDS) is a randomized, embedded, multifactorial, adaptive platform trial for ARDS. The study aimed to assess the impact of multiple interventions on outcomes in patients with ARDS admitted to the ICU.
Mortality is significantly higher in ARDS patients requiring intensive care unit (ICU) admission. ARDS patients admitted to the ICU typically receive multiple (as many as 10 or 20) treatments that work together to fight infection, reduce pulmonary exudation, improve oxygenation, and support systemic organ function. Clinicians are often willing to choose the exact or considered safe and effective regimen from the therapies mentioned above. Still, there are individual differences in ARDS patients, and it is difficult to confirm the optimal treatment plan. It is inevitable to choose treatment without evidence-based medicine based on experience. The primary purpose of this study was to help physicians select the best-effective approach among existing ARDS therapies, and secondly to provide a rationale for specific empirical or emerging ARDS treatments. Clinical evidence to guide optimal management is best obtained from randomized controlled trials (RCTs); however, ARDS is a multi-causal, clinically and therapeutically heterogeneous clinical syndrome with rapid disease progression and complex clinical manifestations, in fact, difficult to organize RCT trials. In cases where the timing of onset and the pathophysiological mechanism cannot be determined, the initial treatment is the selection of protective ventilation/controlled infusion as the first-line standard therapy according to the Berlin classification of ARDS, and some second-line treatments with potential clinical benefit. It is difficult to conduct objective, scientific and timely evaluation, and the overall treatment plan is inevitably blind and empirical. This clinical operation mode is likely related to ARDS-related RCT research results. The results are unsatisfactory, the treatment response heterogeneity is high, and the outcome events vary greatly. closely related to the clinical status. The adaptive platform trial PETARDS is ideal for evaluating the effects of highly heterogeneous ARDS treatment strategies. This clinical research design (adaptive platform trial, APT) can use the information of patients who are participating in the study to guide the clinical treatment of subsequent newly enrolled patients. The APT trial randomized patients into multiple domains for multiple interventions to assess their effectiveness in different patients. The term "domain" refers to a common treatment unit (eg, steroid therapy) within which patients can be randomly assigned to several interventional (dose) groups (including controls, such as no steroids, as appropriate). Certainly). All trial procedures consist of a primary or "core" protocol and multiple secondary protocols, and the standard protocols, clinical treatment adaptations, and trial management and practices for specific treatment units are managed in a unified manner for each treatment unit. The core protocol, secondary protocols, and Statistical Analysis Plan (SAP) of this trial are presented in the appendix; the study required approval from the relevant ethics committees of all participating hospitals and was conducted by good clinical practice guidelines and principles described in the Declaration of Helsinki.
Interventions
DEVICE
Patients with moderate to severe ARDS received ventilation treatment according to predicted body weight(PBW) and controlled plateau pressure.
BEHAVIORAL
patients with moderate to severe ARDS who don't have contraindications were given prone ventilation for over 12 hours.
DRUG
Dexamethasone: Patients received intravenous dexamethasone 20 mg daily from days 1 to 5, reduced to 10 mg daily from days 6 to 10. Hydrocortisone:For septic ARDS patients, 50 mg of hydrocortisone was given as an intravenous bolus every 6 hours for 7 days; For patients with COVID-19-related ARDS, The corticosteroid field randomized participants to a fixed 7-day period of intravenous hydrocortisone (50 mg or 100 mg every 6 hours).
OTHER
1. without other organ dysfunction patients: Minimize fluid was given; 2. other ARDS patients: In the resuscitation phase, controlled fluid replacement combined with vasoactive drugs was given; multiple measures were taken, like lactate and so on, to utilizedto guide fluid resuscitation therapy; diuretics or diuretics in combination with albumin to achieve fluid balance.
BIOLOGICAL
People received thymosin Alpha subcutaneous injections, twice a week.
DRUG
Deep sedation combined with intermittent bolus injection of muscle relaxant or deep sedation combined with continuous infusion of muscle relaxant
OTHER
1. ventilation; 2. conventional western medicine treatment; 3. Chinese herbal medicine(Determining medication based on syndrome differentiation)
DRUG
1. Simvastatin: 80mg qd po for not more than 28days; 2. Rosuvastatin: 20mg qd po (40mg for the first time) for 28days or 3 days after transfer out of the ICU, or the patient died.
COMBINATION_PRODUCT
According to "Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021".
DEVICE
1. For severe ARDS patients with refractory hypoxemia within 7 days of onset; 2. (Inspiratory oxygen concentration) ≥ 0.80, tidal volume 6ml/kg (PBW), positive end-expiratory pressure \[PEEP\] ≥ 10 cmH2O; 3. V-V Model.
GENETIC
A single injection of bone marrow stem cells, doses of 1, 5, 10\*106 cells/kg was taken according to the previous clinical studies.
DRUG
Deep sedation combined with intermittent bolus injection of muscle relaxant or deep sedation combined with continuous infusion of muscle relaxant
Timeline
First posted
Dec 21, 2022
Study start
Oct 1, 2022
Primary completion
Oct 2023
Study completion
Dec 2023
Results posted
Not reported
Registry updated
Dec 21, 2022
Outcomes
ventilator-free days
Time frame · within 28 days
Ventilator-free days 28 days after randomization, definition: Survival without mechanical ventilation
Clinical status assessment
Time frame · 15 days
Patients' clinical status (6-point scale score) was assessed on day 15 after randomization, Definition: This scale ranges from 1 (no hospitalization) to 6 (death), with higher scores indicating worse outcomes.
All-Cause Mortality
Time frame · within 28 days
All-cause mortality 28 days after randomization
Duration of mechanical ventilation
Time frame · within 28 days
days of mechanical ventilation
Sequential Organ Failure Assessment (SOFA) Score
Time frame · at 48 hours, 72 hours, and 7 days after randomization
SOFA Score for different times, from 0 to 24 points
ICU stay time
Time frame · within 90 days
The time for patients staying in ICU when they were in the hospital.
Hospital stay
Time frame · within 90 days
The whole time patients lived in the hospital, including the time when they lived in the ICU
Organ failure free days
Time frame · within 28 days
Patients got ARDS, but the other organs were not injury.
Health-related quality of life assessment, EQ5D-5L and WHODAS 2.0
Time frame · within 6 months
Patient's life quality was assessed according to EQ5D-5L. If the patient had severe impairment of organ function within 6 months, evaluated the patient's quality of life according to WHODAS 2.0
Proportion of intubated patients undergoing tracheostomy
Time frame · 28 days
ARDS patients received tracheostomy.
Where the patient went after discharge
Time frame · No recurrence within 90 days
Home, rehabilitation hospital, nursing home or long-term care facility, or other emergency hospital
Eligibility
Inclusion Criteria: Adult patients (18 years and older, regardless of gender) admitted to the ICU with ARDS; Intubation and mechanical ventilation; Moderate/severe ARDS defined by Berlin criteria (PaO2/FiO2 ≤200mmHg, PEEP ≥5cmH20); Moderate/severe ARDS less than 48 hours before randomization. Exclusion Criteria: Pregnancy or breastfeeding; Known allergy to the intervention drug; Daily use of an intervention drug or measure within the past 15 days; Intervention drugs or measures primarily intended to treat other conditions (eg, septic shock); Patients using the intervention drug or standard for two or more days during hospitalization; Patients are expected to die within the next 24 hours; Other: Participated in PETARDS in the past 90 days.
Study locations
China. Showing up to 24 locations stored in the fast local snapshot.
Peking Union Medical College Hospital
Beijing, China
West China Hospital,Sichuan University
Chengdu, China
Guangdong Provincial People's Hospital
Guangdong, China
The Second Affiliated Hospital of Harbin Medical University
Harbin, China
Lanxi People's Hospital
Lanxi, China
Ningbo First Hospital
Ningbo, China
Zhognshang hospital, Fudan University
Shanghai, China
Taizhou Hosptial of Zhejiang Province
Taizhou, China
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, China
Wuhan University Renmin Hospital
Wuhan, China
The First Affiliated Hospital of Zhengzhou University
Zhengzhou, China
Publications
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