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NCT06410820Completed

Ultrasound Guided Versus Land-mark Method for Spinal Anesthesia in Super Obesity Parturients

Comparison of Ultrasound and Anatomical Landmark Method in Spinal Anesthesia for Elective Cesarean Section in Super Obese Parturients With BMI ≥ 50 kg/m2. A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 25 Feb 2026

Brief summary (registry, in English)

This study will investigate whether an ultrasound-assisted technique is better than a classical land-mark technique to facilitate spinal anesthesia in the sitting position in super obese pregnant women with BMI ≥ 50 who will undergo elective cesarean section. The primary objective of this study is the rate of successful dural puncture at the first attempt. It was assumed that ultrasound could facilitate neuraxial blockade in super obese (BMI ≥ 50 kg/m2), pregnant women, according to the Who classification, whose topographic anatomy is difficult.

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
4 Apr 2024
Start date
16 May 2024
Primary completion date
28 Nov 2025
Lead sponsor
Karaman Training and Research Hospital
Diseases
Obesity
NCT number
NCT06410820

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 16 May 2024 to the primary completion date, 28 Nov 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

  • Local anesthetics allergy
  • History of lumbar spinal diseases and lumbar surgery

Other

  • Multiple gestations
  • Emergency C-section
  • Exist contraindications of spinal anesthesia
  • BMI\<50 kg/m2
  • Parturient refusal

Who the study is looking for

  • Parturient who will receive selective cesarean delivery under spinal anesthesia
  • ASA 3 scheduled for elective sections
  • BMI≥50 kg/m2
  • Normal singleton pregnancy
    • 37 weeks of gestation

Age in the registry: 18 years to 45 years · Sex: Female · Accepts 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
Karaman Training and Research Hospital
Coordinator of this site? Confirm its status
KaramanTurkey (Türkiye)Unknown status

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