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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06415253
Other study ID # MAIEAH630003
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 31, 2023
Est. completion date May 1, 2024

Study information

Verified date May 2024
Source Sanliurfa Mehmet Akif Inan Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Postoperative pulmonary complications are relatively common in all age groups and are closely related to increased costs, morbidity and mortality in the postoperative period. In recent years, various risk indices have been developed for preoperative evaluation to predict postoperative pulmonary complications, such as the American Society of Anaesthesiologists Physical Status Classification (ASA), the Assessment of Respiratory Risk in Surgical Patients in Catalonia (ARISCAT). The ARISCAT score has demonstrated promising results in identifying patients at higher risk for pulmonary complications. The ARISCAT risk index is derived from multiple variables, including age, oxygen saturation, previous respiratory tract infections, anaemia, abdominal or thoracic surgery, operative time, and emergency surgery. The ARISCAT risk index is used to predict respiratory failure, bronchospasm, respiratory tract infections, atelectasis, pneumothorax, pleural effusion, and aspiration pneumonia. Percutaneous nephrolithotomy (PNL) is a type of operation performed endoscopically in a prone position in cases of kidney stones that cannot be broken by extracorporeal shockwave lithotripsy (ESWL) and/or cannot be removed by ureterocystoscopy. The prone position is one of the positions that limits lung capacity and respiratory function. The objective of this study was to assess the relationship between the ARISCAT score in patients undergoing PNL and the occurrence of pulmonary complications in the postoperative period.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date May 1, 2024
Est. primary completion date May 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - American Society of Anesthesiologists (ASA) I-III patients - Patients who undergone of Percutaneous Nephrolithotomy procedure Exclusion Criteria: - Patients with any liver and/or kidney failure - Obese patients (body mass index (BMI) 30 and above) - Trauma patients - Cancer patients - American Society of Anesthesiologists (ASA) IV patients - Cardiac arrhythmia, implanted pacemakers - A history of chronic pain

Study Design


Locations

Country Name City State
Turkey University of Health Science Turkey Sanliurfa Mehmet Akif Inan Training and Research Hospital Sanliurfa

Sponsors (1)

Lead Sponsor Collaborator
Sanliurfa Mehmet Akif Inan Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary rate of pulmonary complication rate of pulmonary complication such as respiratory failure, bronchospasm, atelectasis, pneumothorax, pleural effusion, or aspiration pneumonia. The postoperative period in the first 24 hours
Primary rate of lung infection rate of pneumonia (bacterial or virutic) The postoperative period in the first 72 hours
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