ClinicalTrials.gg
Not yet recruitingNCT07723690Updated Jul 23, 2026

Ultrasonographic Abdominal Fat Thickness and Driving Pressure During Prone Spinal Surgery

An observational study in Respiratory Mechanics, sponsored by Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey. Not yet recruiting. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-07-23.

Sponsored by Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
120
Ages
18 Years to 65 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Respiratory Mechanics
03

In context

Lead sponsor

Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey is the lead sponsor of 108 studies on the registry; 31 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult patients undergoing elective spinal surgery in the prone position under general anesthesia at a single tertiary care hospital.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Adults aged 18 years or older Elective spinal surgery General anesthesia Prone position I-III 18.5-39.9 kg/m²

Exclusion criteria

Exclusion Criteria:

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

Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
120 participants (estimated)
Patient registry
No

Groups and cohorts

  • Adult patients undergoing elective prone spinal surgery

    Adult patients undergoing elective spinal surgery in the prone position under general anesthesia. Preoperative ultrasonographic abdominal subcutaneous fat thickness and intraoperative respiratory mechanics will be evaluated.

06

What researchers measure

Primary outcomes

  1. Intraoperative Driving Pressure

    Time frame: 10 minutes after prone positioning, before surgical manipulation

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jul 2026; primary completion for Nov 2026, 4 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 19, 2026
First posted
Jul 23, 2026
StartEst.
Jul 30, 2026
Primary completionEst.
Nov 30, 2026
CompletionEst.
Nov 30, 2026
Last update
Jul 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07723690
Responsible party
Yadigar Yılmaz (MD, Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey) — Principal investigator
First posted
Jul 23, 2026
Start date
Jul 30, 2026 (estimated)
Primary completion
Nov 30, 2026 (estimated)
Completion
Nov 30, 2026 (estimated)
Last update
Jul 23, 2026

Study contacts

yadigar YILMAZ
Contact
dryadigaryilmaz@gmail.com
0090 (216) 542 2020

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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