Direct Versus Video Laryngoscopy in Patients With Acromegaly

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMuzaffer GENCER

About this trial

Acromegaly is associated with craniofacial skeletal changes and upper airway soft tissue hypertrophy, which may increase the risk of difficult laryngoscopy and tracheal intubation. This prospective observational study aims to evaluate airway and intubation characteristics in patients with acromegaly undergoing surgery under general anesthesia and to compare direct laryngoscopy and video laryngoscopy findings.

Adult patients with acromegaly and patients with nonfunctioning pituitary adenomas scheduled for surgery under general anesthesia will be prospectively enrolled between July 1, 2026, and August 31, 2026. Preoperative airway assessment parameters, hormonal data including growth hormone and insulin-like growth factor-1 levels, Mallampati score, modified Cormack-Lehane grade, intubation-related variables, and peri-intubation complications will be recorded.

Eligibility criteria

Qualifiers

Age 18 years or older

Diagnosis of acromegaly and scheduled for surgery after evaluation by the institutional pituitary diseases council

Diagnosis of nonfunctioning pituitary adenoma and scheduled for surgery after evaluation by the institutional pituitary diseases council

Requirement for general anesthesia with endotracheal intubation

Disqualifiers

Age younger than 18 years

Refusal to participate in the study

Presence of extrapituitary malignancy

Emergency surgery

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

40 Participants
are grouped into 2 trial groups

Locations

This trial has no locations

Sponsors and collaborators

Muzaffer GENCER

Lead sponsor

Başakşehir Çam & Sakura City Hospital

Sponsor institution

Başakşehir Çam & Sakura City Hospital

Collaborator