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Respiratory Distress Syndrome, AdultNCT02664090

Hemodynamic Assessment With Trans-esophageal Doppler (TED) During Prone Ventilation in ARDS Patients

An observational study of Respiratory Distress Syndrome, Adult, run by Sanjay Gandhi Postgraduate Institute of Medical Sciences at 1 site in India.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Acute respiratory distress syndrome (ARDS) commonly complicates acute illness in ICU. This syndrome is associated with high morbidity and mortality. In management of ARDS patients, lung protective ventilation and prone ventilation are key strategies which have shown survival benefits in recent years. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Respiratory Distress Syndrome, Adult
How many people
26 participants
Where
1 siteIndia
Study dates
20 Jan 2016to 18 Jan 2017
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: All critically ill adult patients with diagnosis of ARDS whose hemodynamic monitoring is being done by trans-esophageal doppler (TED), and planned for prone ventilation by treating physician's decision, will be screened for inclusion in this study.

Who may be able to join

  • Adult patients (age > 18 years) with ARDS undergoing prone ventilation

Who cannot join

  • Patients with age <18 years.
  • Conditions which can interfere with interpretation of hemodynamic parameters through TED (aortic coarctation, severe aortic stenosis, severe aortic regurgitation, severe scoliosis)
  • Pregnant patients

Trial locations and contacts

1 site in 1 country.

India1 site
  • Department of Critical Care Medicine

    Lucknow, Uttar Pradesh, 226014

Other trials in India

About this study

Official title: Hemodynamic Assessment With Trans-esophageal Doppler (TED) During Prone Ventilation in Patients With Acute Respiratory Distress Syndrome (ARDS)

Acute respiratory distress syndrome (ARDS) commonly complicates acute illness in ICU. This syndrome is associated with high morbidity and mortality. In management of ARDS patients, lung protective ventilation and prone ventilation are key strategies which have shown survival benefits in recent years. Prone positioning has been reported to have hemodynamic disturbances like hypotension and arrhythmias. The literature till date is unclear with regards to acute hemodynamic changes which can happen during initiation of prone ventilation ,with a few studies suggesting decreasing cardiac output and a few increasing cardiac output. In recent years, trans-esophageal Doppler (TED) has become one of important hemodynamic assessment tool due to its minimal invasiveness, ease of use with its clinical utility established by various studies both in operation theatres and intensive care units. In current study, the investigators would like to evaluate acute hemodynamic effects of prone ventilation with TED in patients of acute respiratory distress syndrome (ARDS).

Read the detailed description

Introduction and rationale of the study:

Acute respiratory distress syndrome (ARDS) commonly complicates acute illness in intensive care units (ICU). This syndrome is associated with high morbidity and mortality. In management of ARDS patients, lung protective ventilation and prone ventilation are key strategies which have shown survival benefits in recent years and now becomes standard part of care in these patients. Prone positioning has been reported to have hemodynamic disturbances like hypotension and arrhythmias. Prone ventilation can have different cardiovascular effects with a few suggesting increased cardiac output and few decreased cardiac output with unclear literature till date with one recent study suggesting that patients who have preload reserve had increased cardiac output when compared to patients with no preload reserve.

In ICU, hemodynamic monitoring is being done as a part of standard care of management in critically ill patients. There are different modalities of continuous hemodynamic monitoring, which help in timely assessment and appropriate interventions to optimize cardiac output to maintain adequate organ perfusion in these critically ill patients. Cardiac output could be assessed by thermo-dilution technique with pulmonary artery catheter, pulse contour analysis of arterial waveform or echocardiography. In recent years, trans-esophageal Doppler (TED) has become one of the standard hemodynamic assessment tool in ICU due to its minimal invasiveness and easy to use. TED uses Doppler shift principle which is routinely used to measure cardiac output in both trans-thoracic and trans-oesophageal echocardiography. The clinical utility of TED, with the benefit of minimal invasiveness, in assessing hemodynamic perturbations in both operation theatre and ICU has been established by various studies. Doppler measured cardiac output showed high validity and clinical agreement with gold standard pulmonary artery thermo-dilution technique, which is more invasive. Hemodynamic assessment in prone position with TED has been studied intra-operatively with good correlation. In current study, the investigators will evaluate acute hemodynamic effects of prone ventilation with TED in patients of acute respiratory distress syndrome (ARDS).

Work plan methodology:

This will be a prospective, observational study, to be conducted in 12 bedded ICU of department of Critical Care Medicine, Sanjay Gandhi Institute of Postgraduate and Medical Sciences, Lucknow. Patients with ARDS whose hemodynamic monitoring is being done by TED, and planned for prone ventilation by treating physician's decision, will be screened for inclusion in this study.

After informed consent from patient's family member for inclusion in the study, demographic data including age, sex, weight, height and ideal body weight (IBW) will be noted. All study participants will have trans-thoracic echocardiography done before inclusion to exclude conditions that can interfere with oesophageal doppler readings like aortic coarctation, severe aortic stenosis, or severe aortic regurgitation. Hemodynamic monitoring with TED (Cardio Q) in these patients will be decided and initiated by treating clinician. As a part of standard treatment for ARDS, all patients will be receiving lung protective ventilation strategies as per ARDS net protocol with appropriate sedation, and also these patients will have relevant invasive and non-invasive vitals monitoring as per ICU protocol.

After decision for prone ventilation by treating clinician and obtaining consent for inclusion in this study, prior to any parameter measurement during study period, probe position of TED will be verified to ensure optimal acquisition of maximum velocity signal. Baseline hemodynamic and respiratory parameters (T1) will be noted in 45 degree head elevation position. Second set (T2) of hemodynamic parameters will be noted after passive leg raise test (PLR). Third set (T3) of hemodynamic parameters in supine position along with IAP measurement.

All ARDS patients will be proned as per ICU protocol, with protective measures for eyes, extended arms, and using appropriate thoraco-pelvic supports for unloading the abdomen and taking all other precautions required for prone positioning. After proning, transducers for invasive monitoring will be re-zeroed relative to atmospheric pressures.

Fourth set (T4) of parameters (hemodynamic) 5 minutes after prone ventilation will be noted. While, fifth set (T5) of parameters (hemodynamic, respiratory and IAP) will be noted 10 minutes after prone ventilation. Subsequently, hemodynamic parameters will be noted at 20 minutes (T6) and the last set (T7) of parameters (hemodynamic and respiratory) will be noted 30 minutes after initiation of prone ventilation.

Sample size calculation: Sample size was calculated by power analysis using PASS 2008 software, with difference in means of cardiac output of 0.6 litre/minute/meter2 between two paired groups and with 95% confidence interval (CI) and 80% power of the study, 22 patients will require. So, the investigators planned to include 25 patients for our study.

Data collection: Demographic and clinical characteristics (ventilatory and hemodynamics) of all included patients will be collected on structured proforma. ICU prognostication scores, i.e., Acute Physiologic and Chronic Health Evaluation (APACHE) II score and Sequential Organ Dysfunction Assessment (SOFA) will also be recorded. From baseline parameters noted before turning the patient prone and after PLR, hemodynamic, ventilatory parameters at sequential time intervals will be noted down until thirty minutes after initiation of prone ventilation.

Intervention: Nil. All patients will be managed as per the ICU treating team's decision

Keywords
acute respiratory distress syndrome, prone ventilation, trans-esophageal doppler
Medical subject headings
Respiratory Distress Syndrome

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To measure pattern of changes in cardiac index (L/min/m2) from baseline (pre-prone position) to during prone position.

    Measured: Baseline (pre-prone) and after initiation of prone-ventilation at 5, 10, 20 and 30 minutes.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jan 2016 (estimated)
  2. Study start20 Jan 2016
  3. Primary completion18 Jan 2017
  4. Study completion18 Jan 2017

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
26 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02664090
Sponsor's protocol ID
2015-139-DM-88
Status last verified
Sep 2019
First submitted
15 Jan 2016
Last updated
25 Sep 2019
Results posted
No
Data monitoring committee
No

Publications

  • Saran S, Gurjar M, Azim A, Mishra P, Ghosh PS, Baronia AK, Poddar B, Singh RK. Trans-Esophageal Doppler Assessment of Acute Hemodynamic Changes Due to Prone Positioning in Acute Respiratory Distress Syndrome Patients. Shock. 2019 Oct;52(4):e39-e44. doi: 10.1097/SHK.0000000000001290.

    PubMed 30475331

Questions about this trial

What is this clinical trial studying?

An observational study of Respiratory Distress Syndrome, Adult, run by Sanjay Gandhi Postgraduate Institute of Medical Sciences at 1 site in India.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 25 Sep 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in India. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To measure pattern of changes in cardiac index (L/min/m2) from baseline (pre-prone position) to during prone position. (time frame: Baseline (pre-prone) and after initiation of prone-ventilation at 5, 10, 20 and 30 minutes.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02664090, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Sep 2019.

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