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NCT07496788Not yet recruiting

Investigation of the Role of Internal Jugular Vein Collapsibility Index in Predicting Spinal Anesthesia-Induced Hypotension in Preeclamptic Parturients

Source: ClinicalTrials.gov · Last updated 27 Mar 2026

Brief summary (registry, in English)

This prospective, single-center observational study aims to evaluate the predictive value of the internal jugular vein collapsibility index (IJVCI) for spinal anesthesia-associated hypotension in preeclamptic parturients (gestational age ≥28 weeks) undergoing cesarean delivery classified as Lucas category 3-4. Preoperative IJVCI will be measured using ultrasonography before spinal anesthesia during spontaneous and deep respiration. The incidence of hypotension within the first 20 minutes after spinal anesthesia will be recorded. The diagnostic performance of IJVCI in predicting hypotension will be analyzed.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
96 (estimated)
First submitted
23 Mar 2026
Start date
1 May 2026
Primary completion date
25 Jul 2026
Lead sponsor
Ankara City Hospital Bilkent
NCT number
NCT07496788

What you commit to

  • Study type: Observational
  • Planned participants: 96
  • From 1 May 2026 to the primary completion date, 25 Jul 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

  • Known renal disease
  • Cardiac instability or known arrhythmia

Age

  • Gestational age \<28 weeks

Other

  • Cesarean urgency classified as Lucas category 1-2
  • ASA physical status ≥ IV
  • Requirement of general anesthesia or sedation
  • Inability to provide informed consent

Who the study is looking for

  • Age between 18 and 45 years
  • ASA physical status II-III
  • Diagnosed with preeclampsia
  • Scheduled for cesarean delivery under spinal anesthesia with cesarean urgency classified as Lucas category 3-4
  • Gestational age ≥28 weeks
  • Provided written informed consent

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Ankara Bilkent City Hospital
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

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