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Trendelenburg as a First-line Intervention in Critically Ill, Sedated, Invasively Mechanically Ventilated, Hypotensive Patients (Trend)

Primary Purpose

Hypotension, Shock

Status
Recruiting
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Trendelenburg position
Semirecumbent position
Sponsored by
Negovsky Reanimatology Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypotension focused on measuring Trendelenburg position, hypotension, hypovolemic shock, shock, head-down position

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age >18 years
  • Admitted to the intensive care unit (ICU);
  • Invasive mechanical ventilation;
  • Pharmacological sedation;
  • Mean arterial pressure (MAP)<65 mmHg or need of fluids infusion or any vasopressor in order to keep MAP > 65 mmHg
  • No contraindication to Semirecumbent or Trendelenburg position;
  • Ongoing monitoring: invasive and non-invasive arterial blood pressure; central venous line with central venous pressure (CVP) monitoring
  • Naso-gastric tube in situ
  • Indwelling bladder catheter
  • Trendelenburg or passive leg raising test responder
  • Consent according to local ethical committee rules

Exclusion Criteria:

  • COPD gold>3,
  • Obesity>grade 2
  • Severe hypoxemia (P/F <100) which can be worsened by diaphragm rise
  • Documented or suspected increased intracranial pressure, based on medical history or actual clinical condition (es. intracranial tumor, cerebral hemorrhage, encephalitis,...);
  • Intra-abdominal hypertension > 2 grade (>20 mmHg)
  • Full stomach pyloric incontinence;
  • Gastric stasis, defined as aspiration from the NG tube of fecal, bloody or green fluid >100mL;
  • Documented or suspected increased intraocular pressure (any degree of glaucoma);
  • No central line inserted or femoral central line only
  • Known diaphragm lesions or hiatus hernia
  • Ischemia of the lower limbs;
  • Upper body fracture;
  • Demand of specific postures after Trauma;
  • Patients who are not able to be investigated with a leg raising test, such as the lower extremities fractures, backbone fractures or backbone pain or deformity, and those patients with large cannulas in the femoral vessels…
  • Any device which, according to the clinician, makes it unfeasible or unsafe to put patients in the Trendelenburg position.
  • Mechanical Circulatory Support;
  • (CHD) (Gleen, Fontaine);
  • Advanced right ventricular dysfunction or advanced cardiac failure, in which volume overload worsens cardiac function (plateau stage in the Frank-Starling curve);
  • Patients planned to be pronated within 6 h;
  • Drainage in thoracic cavity;
  • Upper gastrointestinal bleeding.
  • Ongoing enteral nutrition

Sites / Locations

  • Demikhov Municipal Clinical Hospital 68Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Trendelenburg position

Semirecumbent position

Arm Description

Position: 10-degree Head-down position

Position: 30-degree Head-up position

Outcomes

Primary Outcome Measures

Time to severe hypotension resolution
Time from randomization to timepoint in which MAP > 65 mmHg not requiring fluids or vasoactive drugs (VIS < 5), lasting > 1 hour, in the semirecumbent position

Secondary Outcome Measures

Ventilator-free days at 28 days
28 days - number of days in which the mechanical lung ventilation was not used
ICU-free days at 28 days
28 days - number of days in which the patient was not in an intensive care unit
Restarting vasopressor/inotrope therapy
Using vasopressors and/or inotropes to maintain MAP ≥ 65 mm Hg after premature study termination (Vasoactive inotrope score > 5)
28-days mortality
all cause mortality
90-days mortality
all cause mortality
Acute kidney injury
number of patients who have acute kidney injury according to KDIGO classification
Acute liver failure
Rapid hepatic injury with coagulation derangements and hepatic encephalopathy and multi-organ failure in a patient with no history of liver disease
Ventilation-associated pneumonia
Pneumonia due to mechanical lung ventilation

Full Information

First Posted
January 13, 2022
Last Updated
November 8, 2022
Sponsor
Negovsky Reanimatology Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05209737
Brief Title
Trendelenburg as a First-line Intervention in Critically Ill, Sedated, Invasively Mechanically Ventilated, Hypotensive Patients
Acronym
Trend
Official Title
Trendelenburg as a First-line Intervention in Critically Ill, Sedated, Invasively Mechanically Ventilated, Hypotensive Patients: a Pilot Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 31, 2022 (Actual)
Primary Completion Date
September 20, 2023 (Anticipated)
Study Completion Date
October 20, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Negovsky Reanimatology Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A pilot randomized controlled trial to evaluate the efficacy and safety of Trendelenburg position in critically ill patients with hypotension, mainly patients with septic shock and post operative vasoplegia. The main aim is to assess whether Trendelenburg position can improve organ function through a reduction in the need of fluid infusion and dose of vasopressors. Patients will be screened for participation in the study and eventually randomized based on a balanced randomization scheme (1:1) to Trendelenburg position up to 72 hours after intensive care unit (ICU) admission or Semirecumbent position (standard of care).
Detailed Description
Current consensus on circulatory shock management defines shock as a life-threatening, generalized form of acute circulatory failure associated with inadequate tissue perfusion. Recommended interventions to improve perfusion include early hemodynamic stabilization through fluid resuscitation, along with treatment of the cause of shock. If impaired cardiac function results in inadequate cardiac output and tissue hypoperfusion despite fluid therapy, vasopressor agents should be administered. Nevertheless, fluid overload causes multi-organ edema, such as pulmonary edema or hepatic congestion. Moreover, the negative effects of fluid intravenous administrations were also studied on healthy volunteers during the years. Most of them showed the development of lung injury due to fluid administration. In addition, vasopressors are also associated with poor outcomes. Described serious adverse effects include organ ischemia, tachyarrhythmias, and atrial fibrillation, leading to organ dysfunction and mortality. The head-down position, also known as the Trendelenburg position, was originally used by the surgeon Friederich Trendelenburg to improve surgical exposure of pelvic organs. The Trendelenburg position became then a widely popular procedure in managing patients with hypotension and shock. The primary effect of the Trendelenburg position is an increase in cardiac output. Although the short term effect on blood pressure and CO is certain, there is no agreement on its benefit in terms of tissue perfusion and clinical outcome in critically ill hypotensive patients, as nobody has attempted the Trendelenburg position as first line management. To date, the gold standard position for patients in ICU according to the latest ESICM guidelines to prevent ventilator-associated pneumonia is the semirecumbent position. Experts recommend elevating the head of the patient on the bed to a 20-45 degrees position, preferably >30 degrees position. Critically ill patients with hypotension, mainly patients with septic shock and those with post-operative vasoplegia, may be a subgroup of patients, who would benefit from a head-down position if the risks of aspiration pneumonia are minimized. The Trendelenburg position might permit to avoid the deleterious side effects of fluids and vasoconstrictor administration. The idea is that Trendelenburg position can improve organ function through a reduction in the need of fluid infusion and doses of vasopressors in hypovolemic, hypotensive ICU patients and therefore increase ventilator free days. The main aim of this trial is to assess if Trendelenburg position can reduce time to severe hypotension resolution.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypotension, Shock
Keywords
Trendelenburg position, hypotension, hypovolemic shock, shock, head-down position

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Trendelenburg position
Arm Type
Experimental
Arm Description
Position: 10-degree Head-down position
Arm Title
Semirecumbent position
Arm Type
Active Comparator
Arm Description
Position: 30-degree Head-up position
Intervention Type
Procedure
Intervention Name(s)
Trendelenburg position
Intervention Description
A 10-degree head-down position will be used in this group
Intervention Type
Procedure
Intervention Name(s)
Semirecumbent position
Intervention Description
A 30-degree head-up position will be used in this group
Primary Outcome Measure Information:
Title
Time to severe hypotension resolution
Description
Time from randomization to timepoint in which MAP > 65 mmHg not requiring fluids or vasoactive drugs (VIS < 5), lasting > 1 hour, in the semirecumbent position
Time Frame
72 hours
Secondary Outcome Measure Information:
Title
Ventilator-free days at 28 days
Description
28 days - number of days in which the mechanical lung ventilation was not used
Time Frame
28 days
Title
ICU-free days at 28 days
Description
28 days - number of days in which the patient was not in an intensive care unit
Time Frame
28 days
Title
Restarting vasopressor/inotrope therapy
Description
Using vasopressors and/or inotropes to maintain MAP ≥ 65 mm Hg after premature study termination (Vasoactive inotrope score > 5)
Time Frame
28 days
Title
28-days mortality
Description
all cause mortality
Time Frame
28 days
Title
90-days mortality
Description
all cause mortality
Time Frame
90 days
Title
Acute kidney injury
Description
number of patients who have acute kidney injury according to KDIGO classification
Time Frame
28 days
Title
Acute liver failure
Description
Rapid hepatic injury with coagulation derangements and hepatic encephalopathy and multi-organ failure in a patient with no history of liver disease
Time Frame
28 days
Title
Ventilation-associated pneumonia
Description
Pneumonia due to mechanical lung ventilation
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >18 years Admitted to the intensive care unit (ICU); Invasive mechanical ventilation; Pharmacological sedation; Mean arterial pressure (MAP)<65 mmHg or need of fluids infusion or any vasopressor in order to keep MAP > 65 mmHg No contraindication to Semirecumbent or Trendelenburg position; Ongoing monitoring: invasive and non-invasive arterial blood pressure; central venous line with central venous pressure (CVP) monitoring Naso-gastric tube in situ Indwelling bladder catheter Trendelenburg or passive leg raising test responder Consent according to local ethical committee rules Exclusion Criteria: COPD gold>3, Obesity>grade 2 Severe hypoxemia (P/F <100) which can be worsened by diaphragm rise Documented or suspected increased intracranial pressure, based on medical history or actual clinical condition (es. intracranial tumor, cerebral hemorrhage, encephalitis,...); Intra-abdominal hypertension > 2 grade (>20 mmHg) Full stomach pyloric incontinence; Gastric stasis, defined as aspiration from the NG tube of fecal, bloody or green fluid >100mL; Documented or suspected increased intraocular pressure (any degree of glaucoma); No central line inserted or femoral central line only Known diaphragm lesions or hiatus hernia Ischemia of the lower limbs; Upper body fracture; Demand of specific postures after Trauma; Patients who are not able to be investigated with a leg raising test, such as the lower extremities fractures, backbone fractures or backbone pain or deformity, and those patients with large cannulas in the femoral vessels… Any device which, according to the clinician, makes it unfeasible or unsafe to put patients in the Trendelenburg position. Mechanical Circulatory Support; (CHD) (Gleen, Fontaine); Advanced right ventricular dysfunction or advanced cardiac failure, in which volume overload worsens cardiac function (plateau stage in the Frank-Starling curve); Patients planned to be pronated within 6 h; Drainage in thoracic cavity; Upper gastrointestinal bleeding. Ongoing enteral nutrition
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Valery Likhvantsev
Phone
+79036235982
Email
lik0704@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Levan Berikashvili
Phone
+79263308968
Email
levan.berikashvili@mail.ru
Facility Information:
Facility Name
Demikhov Municipal Clinical Hospital 68
City
Moscow
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Levan Berikashvili
Phone
+79263308968
Email
levan.berikashvili@mail.ru

12. IPD Sharing Statement

Plan to Share IPD
No

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Trendelenburg as a First-line Intervention in Critically Ill, Sedated, Invasively Mechanically Ventilated, Hypotensive Patients

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