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NCT07549776Completed

Ultrasound-guided Versus Landmark-based Spinal Anesthesia in Obese Parturients Undergoing Cesarean Section

Ultrasound-guided Versus Landmark-based Spinal Anesthesia in Obese Parturients Undergoing Cesarean Section: a Prospective Comparative Study

Source: ClinicalTrials.gov · Last updated 7 Jul 2026

Brief summary (registry, in English)

Spinal anesthesia is the most commonly used anesthetic technique for cesarean section. However, in obese parturients, identification of the optimal puncture site using anatomical landmark palpation can be challenging because of altered anatomy. Preprocedural ultrasound has been proposed as a tool to improve localization of the puncture site and facilitate neuraxial access. This is a prospective comparative study included 100 obese parturients undergoing cesarean section under spinal anesthesia. Participants were allocated to one of two comparison groups according to the puncture site localization technique: a preprocedural ultrasound group and an anatomical landmark palpation group. The primary outcome is the first-attempt success rate, defined as successful cerebrospinal fluid return after the first needle insertion without needle redirection or a new skin puncture. Secondary outcomes include the number of puncture attempts, needle redirections, need for rescue interventions, incidence of paresthesia and vascular puncture during the procedure, and procedural times.

Status (registry)
Completed
Study type
Interventional
Enrollment
100 (actual)
First submitted
9 Apr 2026
Start date
1 Jul 2025
Primary completion date
1 Jan 2026
Lead sponsor
Instituto Nacional Materno Perinatal, Peru
Diseases
Obesity
NCT number
NCT07549776

What you commit to

  • Study type: Interventional
  • Participants enrolled: 100
  • From 1 Jul 2025 to the primary completion date, 1 Jan 2026
  • 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

  • History of spinal surgery
  • Infection at the puncture site
  • Allergy to local anesthetics

Other

  • Congenital spinal deformities
  • Coagulopathy
  • Emergency cesarean section (NICE category 1)

Who the study is looking for

  • Age ≥ 18 years
  • Pregnant women undergoing cesarean section
  • Body mass index (BMI) ≥ 30 kg/m² at the time of cesarean section
  • Scheduled for cesarean section under spinal anesthesia

Age in the registry: 18 years to - · Sex: Female · 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
National Maternal and Perinatal Institute
Coordinator of this site? Confirm its status
LimaPeruUnknown status

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