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.
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.
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
- Conditions
- Respiratory Distress Syndrome, Adult
- 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.
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.
- First posted26 Jan 2016 (estimated)
- Study start20 Jan 2016
- Primary completion18 Jan 2017
- Study completion18 Jan 2017
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Respiratory Distress Syndrome, AdultStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Sanjay Gandhi Postgraduate Institute of Medical Sciences
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Mohan Gurjar, Sanjay Gandhi Postgraduate Institute of Medical Sciences
- Investigators
- Mohan Gurjar, MD, PDCC, Principal investigator, Sanjay Gandhi Postgraduate Institute of Medical Sciences
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
Study at a glance
From the registry record, last updated by the sponsor on 25 Sep 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Hemodynamic Assessment With Trans-esophageal Doppler (TED) During Prone Ventilation in Patients With Acute Respiratory Distress Syndrome (ARDS)
- ClinicalTrials.gov ID
- NCT02664090
- Acronym / sponsor ID
- 2015-139-DM-88
- Conditions
- Respiratory Distress Syndrome, Adult
- Keywords
- acute respiratory distress syndrome, prone ventilation, trans-esophageal doppler
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 26 participants (actual)
- Lead sponsor
- Sanjay Gandhi Postgraduate Institute of Medical SciencesOther government
- Study start
- 20 Jan 2016 (actual)
- Primary completion
- 18 Jan 2017 (actual)
- Study completion
- 18 Jan 2017 (actual)
- First posted
- 26 Jan 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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).
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
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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.
Key inclusion criteria (1 listed)
- Adult patients (age > 18 years) with ARDS undergoing prone ventilation
Key exclusion criteria (3 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Sep 2019.
- Derived from this study: PubMed 30475331Saran 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.
- Saran S, Gurjar M, Azim A, Mishra P, Ghosh PS, Baronia AK, et. al. 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. PMID:30475331Link provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Mohan Gurjar, MD, PDCC principal investigator
Sanjay Gandhi Postgraduate Institute of Medical Sciences
1 site in 1 country: see every site and its status.
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.