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Clinical Trials in Turkey / NCT07852702
Starting soon Observational

Irrigation Fluid Volume, Tube Cuff Pressure, and Neck Swelling During Shoulder Arthroscopy

NCT07852702 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-10-15
Last updated
2026-10-01

Condition(s) studied

Shoulder ArthroscopyEndotracheal Tube Cuff PressureNeck Soft Tissue Edema

Investigational drug(s) / intervention(s)

Elective Shoulder Arthroscopy

Elective Shoulder Arthroscopy: Participants will undergo elective shoulder arthroscopy in the beach-chair position under general anesthesia with orotracheal intubation as part of routine clinical care. The study will not assign or modify the surgical indication, arthroscopic procedure, patient positioning, irrigation fluid, irrigation pump settings, or anesthesia management. Researchers will observe and record the total irrigation fluid volume and will perform serial endotracheal tube cuff pressure measurements and preoperative and postoperative assessments of anterior neck soft tissue thickness and neck circumference.

Study summary

During shoulder arthroscopy, fluid is pumped into the shoulder to help the surgeon see inside the joint. Some of this fluid can move into the tissues around the shoulder and neck and cause swelling. During general anesthesia, a breathing tube is placed in the windpipe. This tube has a small inflatable balloon, called a cuff, whose pressure may increase when the surrounding tissues swell.

The purpose of this study is to determine whether larger amounts of irrigation fluid used during shoulder arthroscopy are associated with greater increases in breathing tube cuff pressure and neck soft tissue thickness.

About 60 adults undergoing planned shoulder arthroscopy in the beach-chair position will take part. The study will not change the participants' anesthesia, surgery, or treatment. Researchers will record the amount of irrigation fluid used, measure cuff pressure at set times during surgery, and measure the neck before and after surgery using ultrasound and a measuring tape. Sore throat, hoarseness, and other airway symptoms will be assessed after surgery. Participants will be followed until six hours after surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Age 18 to 75 years * American Society of Anesthesiologists physical status I-III * Scheduled for elective shoulder arthroscopy in the beach-chair position under general anesthesia with orotracheal intubation * Able to read and understand Turkish and provide written informed consent Exclusion Criteria: * Emergency surgery * Pregnancy * Preoperative hoarseness, sore throat, or dysphagia * Upper respiratory tract infection within the previous 2 weeks * Tracheostomy, known laryngeal or tracheal disease, or previous major neck surgery or radiotherapy * Anticipated difficult airway, defined as Mallampati class III-IV or difficult airway predicted by the attending anesthesiologist * More than two tracheal intubation attempts or traumatic intubation * Surgery performed in the lateral decubitus position * Intraoperative use of nitrous oxide * Inability to obtain reliable ultrasonographic measurements

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Health Sciences Fatih Sultan Mehmet Training and Research Hospital Scientific Research Istanbul Turkey (Türkiye)

More Fatih Sultan Mehmet Training and Research Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07852702 on ClinicalTrials.gov ↗ ← All trials in Turkey