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NCT06987240Completed

Landmark vs Ultrasound For Combined Spinal Epidural

Comparison Of Ultrasound-Assisted Combined Spinal Epidural Procedure With Anatomical Landmark Method In Obese Patients Undergoing Lower Extremity Surgery

Source: ClinicalTrials.gov · Last updated 28 Nov 2025

Brief summary (registry, in English)

A comparison of two different methods used in routine anesthesia practices will be made for the insertion of a catheter that will be placed at the waist for anesthesia in obese patients who will undergo orthopedic surgery. 60 obese patients aged 40-80, ASA II-III, BMI\>30, who are planned to undergo elective orthopedic lower extremity surgery by placing a combined spinal epidural catheter at Sakarya University Medical Faculty Education and Research Hospital will be included in the study. General anesthesia or regional anesthesia techniques are routinely used in lower extremity surgery in our clinic. When placing a combined spinal epidural catheter, the entry site is determined by looking at anatomical landmarks or using ultrasound. Patients will be divided into two different groups as Anatomical Marking or Ultrasound. Patients in the Ultrasound group will be taken to the block room in our operating room before the operation and a location marking will be performed with Ultrasound in the block room. Patients in the Anatomical Marking group will be brought to a sitting position in the operating room in the operating room and a location marking will be performed by hand examination. After determining the needle entry site, patients in both groups will undergo the Combined spinal epidural catheter placement procedure, which is performed routinely under sterile conditions, and the success rate at the first attempt, total success rates, number of needle redirections, and complications during the procedure will be compared.

Status (registry)
Completed
Study type
Interventional
Enrollment
68 (actual)
First submitted
22 Apr 2025
Start date
1 May 2025
Primary completion date
1 Aug 2025
Lead sponsor
Sakarya University
Diseases
Obesity
NCT number
NCT06987240

What you commit to

  • Study type: Interventional
  • Participants enrolled: 68
  • From 1 May 2025 to the primary completion date, 1 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with anatomical disorders
  • Patients for whom follow-up conditions could not be met

Other

  • Patients with CSEA contraindication
  • ASA IV-V
  • Diagnosed with scoliosis
  • Patients who did not agree to participate in the study

Who the study is looking for

  • ASA II-III
  • BMI\>30
  • Elective orthopedic lower extremity surgery
  • Combined spinal epidural anesthesia (CSEA)

Age in the registry: 40 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sakarya University Hospital
Coordinator of this site? Confirm its status
SakaryaTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.