Health Sciences University Kartal City Hospital
Istanbul, Turkey (Türkiye)
NCT Number: NCT06705595
This clinical trial aims to determine if different local anesthetic application techniques can reduce postoperative sore throat (POST) and manage hemodynamic responses in adult patients undergoing elective thoracic surgery with double-lumen intubation. The main questions it aims to answer are:
* Does inhaled lidocaine or lidocaine applied to the double-lumen tube reduce the incidence and severity of POST? * How do these anesthetic techniques impact hemodynamic stability during surgery?
Researchers will compare three groups-those receiving inhaled lidocaine, lidocaine applied to the tube, and a saline control group-to see if these methods differ in effectiveness.
Participants will:
* Undergo standard preoperative assessment and provide informed consent * Be randomly assigned to receive either inhaled lidocaine, lidocaine applied to the tube, or saline * Have sore throat scores and hemodynamic data recorded at specific intervals after surgery
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Istanbul, Turkey (Türkiye)
This clinical trial is designed to evaluate the effects of two local anesthetic techniques on postoperative sore throat (POST) incidence and hemodynamic responses in patients undergoing elective thoracic surgery with double-lumen tube (DLT) intubation. POST is a common and undesirable outcome following general anesthesia with endotracheal intubation, particularly with DLTs due to their size and dual cuffs, which can increase mucosal irritation. Addressing POST effectively could significantly improve patient comfort, satisfaction, and overall quality of postoperative care.
**Study Protocol Overview:**
Patients meeting eligibility criteria (aged over 18, ASA I-III) will be recruited from Health Sciences University Kartal City Hospital and randomly assigned to one of three groups:
Data Collection:
The primary outcome measure will be the severity of POST, assessed at 2, 6, 12, and 24 hours postoperatively using a throat pain score (0 to 5 scale). Secondary measures will include hemodynamic parameters (heart rate, systolic and diastolic blood pressures) documented before and after lidocaine application, as well as the incidence of postoperative complications such as hypotension, hypoxemia, hypercapnia, nausea, vomiting, and emergence agitation. Trained investigators will collect data in the operating room, recovery room, and patient wards.
Statistical Analysis:
Data will be analyzed using descriptive and inferential statistics. The Kolmogorov-Smirnov test will assess the normality of data distribution. One-way ANOVA and Bonferroni or Tamhane post-hoc tests will be used for normally distributed variables. For non-parametric variables, the Kruskal-Wallis test and Mann-Whitney U test will be applied. Pearson's chi-square or Fisher's exact test will be used to evaluate qualitative variables, with significance set at p < 0.05.
By comparing different application methods, this study aims to determine an effective approach for reducing POST, which could provide guidance for anesthetic practices in thoracic surgery involving DLTs.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive 2 ml of 10% lidocaine delivered via a Tracheo-Spray device to the tracheal mucosa before anesthesia induction.
Before intubation, participants will receive 10% lidocaine spray applied to the distal surface and cuffs of the double-lumen tube (DLT).
Before intubation, participants will receive 1 ml of 0.9% saline applied to the distal surface and cuffs of the double-lumen tube (DLT).
Time frame: 2, 6, 12, and 24 hours after surgery
The severity of POST will be assessed at 2, 6, 12, and 24 hours after surgery using a throat pain score, ranging from 0 (no pain) to 5 (worst imaginable pain).
Time frame: Basal measurements and 5 minutes after intubation.
Hypotension: Defined as a decrease of more than 20% in systolic blood pressure from baseline or < 80 mmHg.
Hypertension: Defined as an increase of more than 20% in systolic blood pressure from baseline or > 120 mmHg.
Time frame: Postoperative 2. 6. 12. and 24. hours
Hypotension: Defined as a decrease of more than 20% in systolic blood pressure from baseline or < 80 mmHg.
Nausea and Vomiting: Incidence and severity of nausea and vomiting after surgery.
Hypoxemia: Defined as SpO2 < 90% or PaO2 < 60 mmHg. Hypercapnia: Defined as PaCO2 > 45 mmHg. Emergence Agitation: The presence and severity of agitation during emergence from anesthesia.
V.K.V. American Hospital, Istanbul
Other
The Effect of Two Different Local Anesthetic Techniques on Hemodynamic Response and Postoperative Sore Throat in Patients Intubated With Double-Lumen Tubes: A Randomized Controlled Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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