Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06276751
Other study ID # E1-23-3870 ptx endtidalco2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 15, 2023
Est. completion date February 13, 2024

Study information

Verified date February 2024
Source Ankara City Hospital Bilkent
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Pneumothorax (PTX) is defined as the accumulation of air in the pleural space. PTX can cause a disruption in the perfusion of lung tissue in the affected area and increase intrathoracic pressure, potentially leading to obstruction of venous return and, consequently, posing a life-threatening condition. Therefore, PTX requiring urgent intervention is a significant concern in emergency departments. End-tidal carbon dioxide (ETCO2) provides insight into carbon dioxide levels resulting from lung perfusion and serves as a respiratory parameter informing the prognosis of various critical illnesses. One of the most important factors determining lung perfusion is the effective lung area. Among the crucial issues for emergency departments are PTX cases, which typically regress following urgent intervention, leading to the establishment of an effective lung area. Hypotheses have been proposed in the literature suggesting that ETCO2 may be affected in PTX cases due to the relationship between effective lung area and ETCO2. In this study, investigetors aimed to investigate changes in ETCO2 levels following tube thoracostomy applied to PTX cases.


Description:

In the study, a GE brand patient monitor (GE Medical Systems Information Technologies, Germany) was used for vital parameters, and a Medtronic brand Capnostream 35 respiratory monitor device (Oridion Medical 1987 Ltd., Israel) was used for ETCO2 measurement. Patients' ETCO2 measurements were performed using a device that measures ETCO2 levels in breaths delivered through the mouth and nose (sidestream measurement). ETCO2 values were measured before tube thoracostomy placement and at 2 and 4 hours after placement. The diagnosis of pneumothorax was confirmed by chest X-ray. Tube thoracostomy was performed by chest surgeons or emergency physicians. Indications for tube thoracostomy were determined by chest surgery doctors. Patients' age, gender, height, weight, vital signs, smoking history, pneumothorax causes, lateral and apex collapse amount (in mm), procedures performed, ETCO2 values before and after tube insertion at 2 and 4 hours, hemogram, biochemistry, and blood gas values were recorded on case report forms. Additionally, patients' lengths of stay were recorded using archive numbers through the hospital automation system. On chest X-ray, a distance greater than 2 cm between the parietal and visceral pleura at the hilum level according to British guidelines or a distance greater than 3 cm from the apex according to American guidelines was defined as a large pneumothorax. Additionally, the percentage of PTX volume for patients was calculated using the Collins method. The PTX percentage was calculated using the formula "%Collins = '4.2 + 4.7(a + b + c)'", where 'a' is the maximum apical interpleural distance, 'b' is the interpleural distance at the midpoint of the upper half of the lung, and 'c' is the interpleural distance at the midpoint of the lower half of the lung. Neutrophil Lymphocyte Ratio (NLR) and Platelet Lymphocyte Ratio (PLR) calculations were performed. The initial ETCO2 (ETCO2-0) was defined as the ETCO2 measured at the emergency department visit. PaCO2 was defined as the partial pressure of carbon dioxide measured with the first blood gas analysis taken at the emergency department visit. After lung expansion, ETCO2 was defined as the average value of ETCO2 measured 2 to 4 hours after tube thoracotomy (ETCO2-1/ETCO2-2, respectively). The increase in ETCO2 after expansion was defined as the increase in ETCO2 after closed tube thoracotomy (ETCO2 increase after drainage = ETCO2 after tube thoracotomy - initial ETCO2). The change from ETCO2-0 to ETCO2-1 was determined as deltaETCO2-1 (ΔETCO2-1), and the change from ETCO2-0 to ETCO2-2 was determined as ΔETCO2-2.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date February 13, 2024
Est. primary completion date February 6, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Patients aged 18 and over - Individuals without comorbidities - Those diagnosed with spontaneous or traumatic pneumothorax - Patients who underwent tube thoracostomy - Individuals without other organ damage or injury Exclusion Criteria: - Patients under 18 years of age or over 65 years of age - Patients who refuse to participate in the study - Pregnant women - Individuals diagnosed with acute/chronic lung disease - Those with a history of advanced heart failure - Individuals with advanced systemic disease - Patients with a history of malignancy (cancer) - Individuals with chronic liver disease - Those using sedative and analgesic neuro-psychiatric drugs - Patients with a history of psychological or neurological disorders - Individuals with acute organ damage or failure

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
End-tidal CO2 monitor
Throughout the study, measurements were taken at 2 and 4 hours after tube thoracostomy was applied to every patient undergoing the procedure.

Locations

Country Name City State
Turkey Ankara Bilkent Sehir Hastanesi Ankara Çankaya

Sponsors (1)

Lead Sponsor Collaborator
Ankara City Hospital Bilkent

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Lee GM, Kim YW, Lee S, Do HH, Seo JS, Lee JH. End-Tidal Carbon Dioxide Monitoring for Spontaneous Pneumothorax. Emerg Med Int. 2021 Jun 14;2021:9976543. doi: 10.1155/2021/9976543. eCollection 2021. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary ETCO2-0 It was defined as the end-tidal CO2 (ETCO2) measured at the emergency department visit. Five minutes have passed since the emergency room application.
Primary ?ETCO2-1 The change in ETCO2-1 compared to ETCO2-0. Two hours after the emergency room application.
Primary ?ETCO2-2 The change in ETCO2-2 compared to ETCO2-0. Four hours after the emergency room application.
Primary ETCO2-1 End-tidal CO2 measured 2 hours after emergency department admission. Two hours after the emergency room application.
Primary ETCO2-2 End-tidal CO2 measured 2 hours after emergency department admission. Four hours after the emergency room application.
See also
  Status Clinical Trial Phase
Recruiting NCT06022081 - Lung Ultrasound Versus Chest Radiography for Detection of Pneumothorax N/A
Recruiting NCT02907866 - Use of Endobronchial Ultrasound Scope (EBUS) Transducer to Identify Pneumothorax-A Feasibility Study
Terminated NCT03034421 - Prevention of Pneumothorax Following Endoscopic Valve Therapy in Patients With Severe Emphysema N/A
Completed NCT02232841 - Electrical Impedance Imaging of Patients on Mechanical Ventilation N/A
Completed NCT02619591 - Comparison Of Chest Ultrasound Techniques To Identify Clinically Significant Pneumothorax N/A
Recruiting NCT05342675 - Effect of Rapid Rollover on Pneumothorax After CT-Guided Lung Biopsy N/A
Recruiting NCT05910112 - Prospective Data Collection on Clinical, Radiological and Patient Reported Outcomes After Pleural Intervention
Completed NCT03656406 - Effect of Lateral Positioning on Bronchial Cuff Pressure of Left-sided Double-lumen Endotracheal Tube During Thoracic Surgery
Active, not recruiting NCT06075836 - AI Assisted Detection of Chest X-Rays
Recruiting NCT03728491 - Education and Training Competences in Thoracic Ultrasound N/A
Recruiting NCT05407974 - Pleurectomy Versus Pleural Abrasion in Patients With Spontaneous Pneumothorax N/A
Completed NCT01670942 - Hypobaria and Traumatic Pneumothorax N/A
Terminated NCT00969423 - Chronic Pain After Video-assisted Thoracoscopic Surgery (VATS) Surgery for Pneumothorax N/A
Completed NCT05904574 - Effectiveness of the Autologous Blood Patch Method in Lung Biopsies
Completed NCT03327688 - Point-of-care Ultrasound in Finland N/A
Completed NCT05963945 - Multi-Reader Retrospective Study Examining Carebot AI CXR 2.0.21-v2.01 Implementation in Everyday Radiology Clinical Practice
Completed NCT05222568 - Effect of the Minimum Bronchial Cuff Volume of Left-sided Double-lumen Endotracheal Tube for One-lung Ventilation on the Change of the Bronchial Cuff Pressure During Lateral Positioning in Thoracic Surgery
Not yet recruiting NCT05121233 - Local Anesthesia Versus Combined Local Anesthesia With Single Dose Analgesia on Pain Control During Thoracic Ultrasound Guided Procedures Phase 4
Completed NCT03064659 - Driving Pressure And EFL in Adult Cardiac Surgery N/A
Recruiting NCT02090205 - Mechanical Ventilation During Cardiac Surgery N/A