Clinical trials

2

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Condition / disease
Location
Status: Recruiting

IVC Collapsibility Index in Lumbar Stabilization Surgery

This study aims to evaluate perioperative hemodynamic changes using the inferior vena cava (IVC) collapsibility index in patients undergoing lumbar stabilization surgery under general anesthesia. The IVC diameter and collapsibility index will be measured using ultrasonography at predefined perioperative time points. Hemodynamic parameters such as blood pressure and heart rate will also be recorded. The study seeks to determine whether the IVC collapsibility index can be used as a non-invasive indicator of intravascular volume status and hemodynamic changes during lumbar spine surgery.

Participants needed: 128
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Trabzon Kanuni Education and Research HospitalUpdated: Apr 23, 2026Locations: 2
Eligibility criteria

Age ≥ 18 years [+4]

Age younger than 18 years [+12]

Status: Recruiting

Comparison of Airway Ultrasonography and Laryngoscopy Methods in Obese Patients

The main objective of this study was to examine the relationship between classical markers used in assessing difficult airway management in obese patients (Mallampati score, thyromental distance, sternomental distance, neck circumference measurement) and ultrasonographic parameters (vocal cord mobility, glottic opening, hyomental distance, skin-epiglottic distance, and peri-epiglottic space-epiglottic-vocal cord ratio), to compare the effects of these parameters on predicting difficult intubation, and to investigate the effects of different laryngoscopy methods on intubation success and peroperative respiratory complications. The secondary objective of the study is to investigate the effects of different laryngoscopy methods on hemodynamic responses to intubation. Participants' gender, age, height, weight, BMI, ASA physical status classification, smoking status, comorbidities, STOP-BANG and LEMON scores will be recorded. The glottic score percentage (POGO score), glottic visualization time, endotracheal intubation time, use of assistive maneuvers, and Intubation Difficulty Scale (IDS) parameters will be compared according to the laryngoscopy methods used. Participants must meet the following criteria: * Consent given by the patient * Operated under general anesthesia * Over 18 years of age * American Society of Anesthesiologists (ASA) physical status classification I-II-III * Body mass index (BMI) of 30 kg/m2 or higher * Operation duration between 60-150 minutes * Patients undergoing elective surgery.

Participants needed: 180
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Trabzon Kanuni Education and Research HospitalUpdated: Mar 19, 2026Locations: 1
Eligibility criteria

Patients who have given their consent [+6]

Patients who do not consent, [+5]