Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05557461
Other study ID # huseyinetco2
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 20, 2022
Est. completion date March 30, 2023

Study information

Verified date January 2023
Source Bozyaka Training and Research Hospital
Contact Hüseyin Özkarakas, MD
Phone 5065873420
Email h.ozkarakas@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Fluid therapy is important in patients with sepsis and septic shock. There are many invasive and non-invasive methods to assess fluid responsiveness in patients. The specificities and sensitivities of these methods are highly variable. The reason for our study was to determine end-tidal co2 and fluid responsiveness in septic shock patients. The aim of the study was to evaluate the fluid response using the End-tidal CO2 difference in septic shock patients receiving intubated mechanical ventilation support.


Description:

End-tidal CO2 is a parameter that can be easily measured with our non-invasively available monitors. If results are positive, fluid response of patients can be measured with a non-invasive, easy-to-apply method. The significance of end-tidal CO2 will be confirmed by the passive leg raise test. Assessment of fluid responsiveness with the passive leg raise test is currently seen as the non-invasive reference test used. It has proven its accuracy and reliability in many studies. In the passive leg raise test, end-tidal CO2 will be compared between the group with and without fluid responsiveness. Scope of the study: Patients hospitalized in the general and reanimation intensive care units of our hospital and diagnosed with septic shock for any reason. Method(s) to be applied: All patients diagnosed with septic shock will be included in the study. The passive leg raise test, will be applied to the patients, and cardiac output and end-tidal CO2 changes will be recorded with transthoracic echocardiography before and after. Fluid responsiveness is considered to be present in patients whose stroke volume variation output change measured by echocardiography increases by 10% or more after the passive leg raise test. Patients will be divided into 2 groups according to fluid responsiveness. Group-1 group with fluid responsiveness in passive leg raise test, Group-2 group with no fluid response in passive leg raise test. End-tidal CO2 will be compared between groups. Passive leg raise test: After the patients are in a semi-sitting position (at least 2 minutes), two healthcare professionals will take the supine position and then lift their legs 45 degrees, wait for 2 minutes and return to the initial position. With this maneuver, it is anticipated that approximately 150-300 ml of autotransfusion will be administered to the patient. Statistical analyzes will be made with the SPSS 21 program. Normally distributed data will be expressed as mean ± standard deviation, non-normally distributed data will be expressed as median. Categorical data will be expressed as a percentage. The difference between the mean and median values will be evaluated according to the distribution of the data by Student's t or Mann-Whitney U test. Categorical data will be evaluated with the chi-square test. A p value <0.05 will be considered significant.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date March 30, 2023
Est. primary completion date February 27, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - over 18 years old - in circulatory shock - Hemodynamically stable for 10 minutes (whether or not he takes vasoactive drugs) - Followed in mechanical ventilation with invasive arterial monitoring Exclusion Criteria: - pregnant - Heart cannot be visualized by echocardiography - Patients for whom passive leg raise test cannot be performed - Bilateral lower extremity amputation - Patients who are hemodynamically unstable

Study Design


Related Conditions & MeSH terms


Intervention

Device:
End-tifdal co2, systolic, diastolic blood pressure, ppv values and vci distensibility
(0,1,3,5 minutes measurements will be taken) measured before and after the test will be recorded and compared. Cardiac output and stroke volume variation, vci distensibility will be measured and recorded by a specialist cardiologist using siemens ocuson cv70 (Siemens AG Medical Solutions, Henkestrasse, the Germany) echocardiography before and after the test.

Locations

Country Name City State
Turkey UHS Izmir Bozyaka Education and Research Hospital Izmir Karabaglar

Sponsors (1)

Lead Sponsor Collaborator
Bozyaka Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (3)

Arango-Granados MC, Zarama Cordoba V, Castro Llanos AM, Bustamante Cristancho LA. Evaluation of end-tidal carbon dioxide gradient as a predictor of volume responsiveness in spontaneously breathing healthy adults. Intensive Care Med Exp. 2018 Jul 30;6(1):21. doi: 10.1186/s40635-018-0187-0. — View Citation

Monnet X, Marik P, Teboul JL. Passive leg raising for predicting fluid responsiveness: a systematic review and meta-analysis. Intensive Care Med. 2016 Dec;42(12):1935-1947. doi: 10.1007/s00134-015-4134-1. Epub 2016 Jan 29. — View Citation

Toupin F, Clairoux A, Deschamps A, Lebon JS, Lamarche Y, Lambert J, Fortier A, Denault AY. Assessment of fluid responsiveness with end-tidal carbon dioxide using a simplified passive leg raising maneuver: a prospective observational study. Can J Anaesth. 2016 Sep;63(9):1033-41. doi: 10.1007/s12630-016-0677-z. Epub 2016 Jun 15. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary end tidal co2 the level of carbon dioxide that is released at the end of an exhaled breath Recording will be made immediately before the passive leg raise test.
Primary end tidal co2 the level of carbon dioxide that is released at the end of an exhaled breath Recording will be made at the 1st minute after the end of the test.
Primary end tidal co2 the level of carbon dioxide that is released at the end of an exhaled breath Recording will be made 3rd minute after the end of the test.
Secondary diastolic blood pressure Recording will be made immediately before the passive leg raise test.
Secondary diastolic blood pressure Recording will be made at the 1st minute after the end of the test.
Secondary diastolic blood pressure Recording will be made 3rd minute after the end of the test.
Secondary systolic blood pressure Recording will be made immediately before the passive leg raise test.
Secondary systolic blood pressure Recording will be made at the 1st minute after the end of the test.
Secondary systolic blood pressure Recording will be made 3rd minute after the end of the test.
Secondary ppv values Pulse pressure variation Recording will be made immediately before the passive leg raise test.
Secondary ppv values Pulse pressure variation Recording will be made at the 1st minute after the end of the test.
Secondary ppv values Pulse pressure variation Recording will be made 3rd minute after the end of the test.
Secondary vci distensibility Distensibility Index of Inferior Vena Cava Recording will be made immediately before the passive leg raise test.
Secondary vci distensibility Distensibility Index of Inferior Vena Cava Recording will be made at the 1st minute after the end of the test.
Secondary vci distensibility Distensibility Index of Inferior Vena Cava Recording will be made 3rd minute after the end of the test.
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05095324 - The Biomarker Prediction Model of Septic Risk in Infected Patients
Completed NCT02714595 - Study of Cefiderocol (S-649266) or Best Available Therapy for the Treatment of Severe Infections Caused by Carbapenem-resistant Gram-negative Pathogens Phase 3
Completed NCT03644030 - Phase Angle, Lean Body Mass Index and Tissue Edema and Immediate Outcome of Cardiac Surgery Patients
Completed NCT02867267 - The Efficacy and Safety of Ta1 for Sepsis Phase 3
Completed NCT04804306 - Sepsis Post Market Clinical Utility Simple Endpoint Study - HUMC
Terminated NCT04117568 - The Role of Emergency Neutrophils and Glycans in Postoperative and Septic Patients
Completed NCT03550794 - Thiamine as a Renal Protective Agent in Septic Shock Phase 2
Completed NCT04332861 - Evaluation of Infection in Obstructing Urolithiasis
Completed NCT04227652 - Control of Fever in Septic Patients N/A
Enrolling by invitation NCT05052203 - Researching the Effects of Sepsis on Quality Of Life, Vitality, Epigenome and Gene Expression During RecoverY From Sepsis
Terminated NCT03335124 - The Effect of Vitamin C, Thiamine and Hydrocortisone on Clinical Course and Outcome in Patients With Severe Sepsis and Septic Shock Phase 4
Recruiting NCT04005001 - Machine Learning Sepsis Alert Notification Using Clinical Data Phase 2
Completed NCT03258684 - Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Sepsis and Septic Shock N/A
Recruiting NCT05217836 - Iron Metabolism Disorders in Patients With Sepsis or Septic Shock.
Completed NCT05018546 - Safety and Efficacy of Different Irrigation System in Retrograde Intrarenal Surgery N/A
Completed NCT03295825 - Heparin Binding Protein in Early Sepsis Diagnosis N/A
Not yet recruiting NCT06045130 - PUFAs in Preterm Infants
Not yet recruiting NCT05361135 - 18-fluorodeoxyglucose Positron Emission Tomography/Computed Tomography in S. Aureus Bacteraemia N/A
Not yet recruiting NCT05443854 - Impact of Aminoglycosides-based Antibiotics Combination and Protective Isolation on Outcomes in Critically-ill Neutropenic Patients With Sepsis: (Combination-Lock01) Phase 3
Not yet recruiting NCT04516395 - Optimizing Antibiotic Dosing Regimens for the Treatment of Infection Caused by Carbapenem Resistant Enterobacteriaceae N/A