Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04286490
Other study ID # 38RC19.265
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 2020
Est. completion date June 2022

Study information

Verified date May 2020
Source University Hospital, Grenoble
Contact Anne-Sophie Truche, M.D
Phone + 33 476768779
Email ASTruche@chu-grenoble.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients suffering from Acute Respiratory Distress Syndrome (ARDS) with a prone position (PP) indication will benefit from measurements of radiological and biological kidney injury markers, intra-abdominal pressure (IAP) and ventilatory mechanics in supine position (baseline IAP), after 2 hours in PP at the current IAP value, thirty minutes after patients' abdomen suspension in order to resume baseline IAP and after patients' are turned back to supine position.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 29
Est. completion date June 2022
Est. primary completion date June 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ARDS patients according to Berlin criteria, intubated, mechanically ventilated since at least 24 hours,

- with PaO2/FiO2 < 150 mmHg,

- neuromuscular blockade

- with an indication of PP done by the physician in charge

- possibility to differ PP for one hour

- patients should be hemodynamically stable since at least 4 hours

Exclusion Criteria:

- Pregnant or breast-feeding women

- legal protection, no social security affiliation

- PP contra-indication

- nasogastric tube contra-indication

- extra corporeal membrane oxygenation

- acute kidney injury at inclusion according to K-DIO criteria, chronic kidney disease defined as an estimated glomerualr filtration rate less than 30 ml/min/1.73m², kidney transplantation, renal artery stenosis, solitary kidney, albuminuria > 1.25 mg/ml

- cardiac arrhythmia

- obesity

- advanced cirrhosis

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Prone position
Abdomen suspension in prone position

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
University Hospital, Grenoble Act For Chronic Diseases, French Society for Intensive Care

Outcome

Type Measure Description Time frame Safety issue
Primary change in renal resistive index (RRI) RRI measurement will be performed on a right kidney arcuate/interlobar artery, with a high frequency Doppler probe. Three to five consecutive measures will be obtained then RRI computed according to the formula: (peak systolic velocity - end diastolic velocity)/peak systolic velocity). At inclusion (in supine position), two hours after prone positioning, 30-minutes after the abdomen suspension maneuver
Secondary change in renal medullary oxygen tension urinary oxygen tension (uPO2) will be measured via a fiber-optic luminescence optode inserted through the bladder catheter lumen At inclusion (in supine position), two hours after prone positioning, 30-minutes after the abdomen suspension maneuver
Secondary change in cell-cycle arrest biomarkers Tissue inhibitor of metalloproteinases 2 and Insulin-like growth factor-binding protein 7 concentrations product ([TIMP2] · [IGFBP7]) will be measured with a sandwich immunoassay technique At inclusion (in supine position), two hours after prone positioning, 30-minutes after the abdomen suspension maneuver
Secondary ventilatory mechanics: transpulmonary pressure transpulmonary pressure will be measured at the end of inspiration and expiration and continuously recorded on a datalogger At inclusion (in supine position), two hours after prone positioning, 30-minutes after the abdomen suspension maneuver
Secondary ventilatory mechanics: driving pressure driving pressure will be measured at the end of inspiration and expiration and continuously recorded on a datalogger At inclusion (in supine position), two hours after prone positioning, 30-minutes after the abdomen suspension maneuver
Secondary ventilatory mechanics: elastance elastance will be measured at the end of inspiration and expiration and continuously recorded on a datalogger At inclusion (in supine position), two hours after prone positioning, 30-minutes after the abdomen suspension maneuver
Secondary haematosis arterial oxygen tension (PaO2) and arterial dioxide carbon tension (PaC02) At inclusion (in supine position), two hours after prone positioning, 30-minutes after the abdomen suspension maneuver
Secondary Intra abdominal pressure Intra abdominal pressure will be measured thanks to a dedicated nasogastric tube with two balloons (gastric pressure) At inclusion (in supine position), two hours after prone positioning, 30-minutes after the abdomen suspension maneuver and two hours after patients are back in supine position
Secondary Persisting effect of IAP increase in prone position when patients are back in supine position on renal resistive index RRI measurement will be performed on a right kidney arcuate/interlobar artery, with a high frequency Doppler probe. Three to five consecutive measures will be obtained then RRI computed according to the formula: (peak systolic velocity - end diastolic velocity)/peak systolic velocity). Two hours after patients are back in supine position
Secondary Persisting effect of IAP increase in prone position when patients are back in supine position on urinary PO2 urinary oxygen tension (uPO2) will be measured via a fiber-optic luminescence optode inserted through the bladder catheter lumen Two hours after patients are back in supine position
Secondary Persisting effect of IAP increase in prone position when patients are back in supine position on cell-cycle arrest biomarkers Tissue inhibitor of metalloproteinases 2 and Insulin-like growth factor-binding protein 7 concentrations product ([TIMP2] · [IGFBP7]) will be measured with a sandwich immunoassay technique Two hours after patients are back in supine position
Secondary Persisting effect of IAP increase in prone position when patients are back in supine position on ventilatory mechanics: transpulmonary pressure transpulmonary pressure will be measured at the end of inspiration and expiration and continuously recorded on a datalogger Two hours after patients are back in supine position
Secondary Persisting effect of IAP increase in prone position when patients are back in supine position on ventilatory mechanics: driving pressure driving pressure will be measured at the end of inspiration and expiration and continuously recorded on a datalogger Two hours after patients are back in supine position
Secondary Persisting effect of IAP increase in prone position when patients are back in supine position on ventilatory mechanics: elastance elastance will be measured at the end of inspiration and expiration and continuously recorded on a datalogger Two hours after patients are back in supine position
Secondary Persisting effect of IAP increase in prone position when patients are back in supine position on haematosis arterial oxygen tension (PaO2) and arterial dioxide carbon tension (PaC02) Two hours after patients are back in supine position
Secondary Acute kidney injury According to creatinine or diuresis criteria of Kidney Disease: Improving Global Outcomes (K-DIGO) classification within 48 hours following prone position
See also
  Status Clinical Trial Phase
Recruiting NCT05538351 - A Study to Support the Development of the Enhanced Fluid Assessment Tool for Patients With Acute Kidney Injury
Recruiting NCT06027788 - CTSN Embolic Protection Trial N/A
Completed NCT03938038 - Guidance of Ultrasound in Intensive Care to Direct Euvolemia N/A
Recruiting NCT05805709 - A Patient-centered Trial of a Process-of-care Intervention in Hospitalized AKI Patients: the COPE-AKI Trial N/A
Recruiting NCT05318196 - Molecular Prediction of Development, Progression or Complications of Kidney, Immune or Transplantation-related Diseases
Recruiting NCT05897840 - Continuous Central Venous Oxygen Saturation Measurement as a Tool to Predict Hemodynamic Instability Related to Renal Replacement Therapy in Critically Ill Patients N/A
Recruiting NCT04986137 - Fractional Excretion of Urea for the Differential Diagnosis of Acute Kidney Injury in Cirrhosis
Terminated NCT04293744 - Acute Kidney Injury After Cardiac Surgery N/A
Completed NCT04095143 - Ultrasound Markers of Organ Congestion in Severe Acute Kidney Injury
Not yet recruiting NCT06026592 - Detection of Plasma DNA of Renal Origin in Kidney Transplant Patients
Not yet recruiting NCT06064305 - Transcriptional and Proteomic Analysis of Acute Kidney Injury
Terminated NCT03438877 - Intensive Versus Regular Dosage For PD In AKI. N/A
Terminated NCT03305549 - Recovery After Dialysis-Requiring Acute Kidney Injury N/A
Completed NCT05990660 - Renal Assist Device (RAD) for Patients With Renal Insufficiency Undergoing Cardiac Surgery N/A
Completed NCT04062994 - A Clinical Decision Support Trial to Reduce Intraoperative Hypotension
Terminated NCT02860130 - Clinical Evaluation of Use of Prismocitrate 18 in Patients Undergoing Acute Continuous Renal Replacement Therapy (CRRT) Phase 3
Completed NCT06000098 - Consol Time and Acute Kidney Injury in Robotic-assisted Prostatectomy
Not yet recruiting NCT05548725 - Relation Between Acute Kidney Injury and Mineral Bone Disease
Completed NCT02665377 - Prevention of Akute Kidney Injury, Hearttransplant, ANP Phase 3
Terminated NCT03539861 - Immunomodulatory Biomimetic Device to Treat Myocardial Stunning in End-stage Renal Disease Patients N/A