Endoscopy Clinical Trials

Clinical trials related to Endoscopy Procedure

Comparison of Peri-intubation Oxygenation Values and Complications in Patients Intubated With the Delayed Sequential Intubation (DSI) Versus Rapid Sequence Intubation (RSI) Protocols

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study compares two different methods of helping patients breathe by placing a tube in their airway (intubation) in an emergency setting. These methods are called Rapid Sequence Intubation (RSI) and Delayed Sequence Intubation (DSI). The study focuses on adult patients who are still breathing on their own but need a breathing tube for medical reasons not related to an injury (non-trauma). The main goal of the research is to compare: * Oxygen levels before and after the procedure. * The patient's vital signs (such as heart rate and blood pressure). * The number of attempts needed to successfully place the tube and the time the procedure takes. * Blood gas results and any complications that occur during or shortly after the procedure. * Early survival (mortality) rates. While there are previous studies on trauma patients or small observational reports, there is currently no large-scale, multicenter randomized controlled trial that includes all non-trauma adult patients. What makes this study unique? Confirmation of Tube Placement: Researchers will use a specific measurement called end-tidal CO2 (etCO2) to confirm the tube is in the right place, a method not used in similar previous studies. Assessing Difficulty: This study will use the Cormack-Lehane classification system to measure how difficult the intubation was for each patient. Standardization: For the first time, breathing machine (ventilator) settings will be standardized for all patients in this type of study. Real-World Practice: By involving all emergency department physicians as practitioners, the study aims to show how these methods work across a wide range of medical teams.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Aged 18 years or older

• Presence of spontaneous breathing.

• No prediction of a difficult airway prior to intubation.

• Requirement for advanced airway management.

• Not in cardiac arrest.

• Decided to intubate due to non-traumatic etiologies.

• Planned intubation using ketamine for sedation and rocuronium for paralysis.

• Decision to intubate due to one of the following clinical conditions:

‣ Acute Respiratory Failure: Patients with hypoxic or hypercapnic respiratory failure where adequate oxygenation cannot be achieved despite non-invasive ventilation.

⁃ Inability to Protect the Airway: Altered level of consciousness or increased risk of pulmonary aspiration due to conditions such as upper gastrointestinal bleeding, ileus, volvulus, gastric outlet obstruction, hypersalivation, or hyperemesis.

⁃ Shock States: Patients in any state of shock (hypovolemic, distributive, cardiogenic, obstructive) exhibiting severe altered mental status or declining respiratory status.

⁃ Neuroprotection: Need to terminate ongoing seizures resistant to medical therapy (status epilepticus), or situations requiring strict control of arterial carbon dioxide (PaCO₂) levels to manage increased intracranial pressure (ICP) in non-traumatic conditions (such as intracranial hemorrhage or severe encephalopathy).

• Obtaining informed consent from the patient or their legally authorized representative.

Locations
Other Locations
Turkey
Basaksehir Cam and Sakura City Hospital
RECRUITING
Istanbul
İstanbul Haseki Training and Research Hospital
RECRUITING
Istanbul
Kanuni Sultan Süleyman Research and Training Hospital
RECRUITING
Istanbul
Şişli Hamidiye Etfal Training and Research Hospital
RECRUITING
Istanbul
Contact Information
Primary
Utku Murat Kalafat, Associate Professor
utkumuratk@yahoo.com
+90-507-262-74-04
Backup
Muhammed Güner, Doctor
muhammedgner@gmail.com
+90-534-765-46-93
Time Frame
Start Date: 2025-10-29
Estimated Completion Date: 2026-06-29
Participants
Target number of participants: 140
Treatments
Experimental: Delayed Sequence Intubation
Active_comparator: Rapid Sequence Intubation
Related Therapeutic Areas
Sponsors
Leads: Kanuni Sultan Suleyman Training and Research Hospital

This content was sourced from clinicaltrials.gov