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Not yet recruiting NCT07723690

Ultrasonographic Abdominal Fat Thickness and Driving Pressure During Prone Spinal Surgery

Observational Respiratory Mechanics

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Respiratory Mechanics. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Association Between Ultrasonographic Abdominal Subcutaneous Fat Thickness and Intraoperative Driving Pressure in Adult Patients Undergoing Elective Prone Spinal Surgery: A Prospective Observational Study

Overview

This prospective observational study aims to evaluate the association between preoperative abdominal subcutaneous fat thickness measured by ultrasonography and intraoperative driving pressure in adult patients undergoing elective spinal surgery in the prone position under general anesthesia. Anthropometric measurements including body mass index, waist circumference, waist-to-height ratio, and neck circumference will also be evaluated for their association with respiratory mechanics. No additional intervention beyond routine clinical care will be performed.

Primary outcome measures

  • Intraoperative Driving Pressure [Time frame: 10 minutes after prone positioning, before surgical manipulation]

Eligibility criteria

Inclusion criteria

Adults aged 18 years or older Elective spinal surgery General anesthesia Prone position ASA physical status I-III Body mass index 18.5-39.9 kg/m²

Exclusion criteria

Emergency surgery Pregnancy Severe restrictive or obstructive pulmonary disease Hemodynamic instability Body mass index <18.5 or ≥40 kg/m² Incomplete study measurements

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07723690 · SAH-2026-107

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗