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Platform Adaptive Embedded Trial for Acute Respiratory Distress Syndrome

Platform Adaptive Embedded Trial for Acute Respiratory Distress Syndrome

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05658692
Acronym
PETARDS
Enrollment
1000
Registered
2022-12-21
Start date
2022-10-01
Completion date
2023-12-31
Last updated
2022-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome

Keywords

ARDS, ICU, domain, platform adaptive embedded trial

Brief 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.

Detailed description

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

DRUGinotropes therapy

According to Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021.

DRUGVasoactive drug therapy

According to Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021.

Patients with moderate to severe ARDS received ventilation treatment according to predicted body weight(PBW) and controlled plateau pressure.

patients with moderate to severe ARDS who don't have contraindications were given prone ventilation for over 12 hours.

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).

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.

BIOLOGICALThymosin Alpha

People received thymosin Alpha subcutaneous injections, twice a week.

DRUGMuscle relaxant therapy

Deep sedation combined with intermittent bolus injection of muscle relaxant or deep sedation combined with continuous infusion of muscle relaxant

OTHERIntegrated Chinese and Western Medicine Treatment

1. ventilation; 2. conventional western medicine treatment; 3. Chinese herbal medicine(Determining medication based on syndrome differentiation)

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_PRODUCTanti-infective treatment

According to Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021.

DEVICEExtracorporeal Membrane Oxygenation(ECMO)

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.

A single injection of bone marrow stem cells, doses of 1, 5, 10\*106 cells/kg was taken according to the previous clinical studies.

DRUGSedative analgesia/muscle relaxant therapy

Deep sedation combined with intermittent bolus injection of muscle relaxant or deep sedation combined with continuous infusion of muscle relaxant

Sponsors

Renmin Hospital of Wuhan University
CollaboratorOTHER
The Second Affiliated Hospital of Harbin Medical University
CollaboratorOTHER
West China Hospital
CollaboratorOTHER
The First Affiliated Hospital of Zhengzhou University
CollaboratorOTHER
Peking Union Medical College Hospital
CollaboratorOTHER
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
CollaboratorOTHER
Fudan University
CollaboratorOTHER
Guangdong Provincial People's Hospital
CollaboratorOTHER
Ningbo No. 1 Hospital
CollaboratorOTHER
Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University
CollaboratorOTHER
Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
ventilator-free dayswithin 28 daysVentilator-free days 28 days after randomization, definition: Survival without mechanical ventilation

Secondary

MeasureTime frameDescription
Health-related quality of life assessment, EQ5D-5L and WHODAS 2.0within 6 monthsPatient'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 tracheostomy28 daysARDS patients received tracheostomy.
Clinical status assessment15 daysPatients' 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 Mortalitywithin 28 daysAll-cause mortality 28 days after randomization
Duration of mechanical ventilationwithin 28 daysdays of mechanical ventilation
Organ failure free dayswithin 28 daysPatients got ARDS, but the other organs were not injury.
ICU stay timewithin 90 daysThe time for patients staying in ICU when they were in the hospital.
Hospital staywithin 90 daysThe whole time patients lived in the hospital, including the time when they lived in the ICU
Where the patient went after dischargeNo recurrence within 90 daysHome, rehabilitation hospital, nursing home or long-term care facility, or other emergency hospital
Re-admission to ICU during readmissionwithin 90 daysPatients were sent to the hospital and sent to the ICU again,
Days not in intensive care unit28 days after randomizationICU transfer and discharge 28 days after randomization
Sequential Organ Failure Assessment (SOFA) Scoreat 48 hours, 72 hours, and 7 days after randomizationSOFA Score for different times, from 0 to 24 points

Countries

China

Contacts

Primary ContactZhaocai Zhang, Doctor
2313003@zju.edu.cn+86-13758131998

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026