Upper vs Lower Extremity BP in Spinal Cesarean Using ClearSight

Recruiting Observational Study
Anesthesia Pregnancy Related Blockades Neuromuscular
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Female
Study type
Observational
Participants needed
327 (estimated)
Sponsor
Ohio State University · Other
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About This Trial
This is a single-center, prospective observational study in patients undergoing cesarean delivery under spinal or combined spinal-epidural anesthesia. It compares whether continuous noninvasive hemodynamic measurements from the lower extremity (toe) better predict neonatal outcomes than upper extremity (arm/finger) measurements during spinal-induced hypotension. Participants receive standard spin…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age ≥ 18 years old * Singleton pregnancy * Gestational age ≥ 37 weeks * Women undergoing CD under SAB or Combined Spinal-Epidural (CSE) electively. * Ability to consent in English and in Spanish language Exclusion Criteria: * CD under or converted to general anesthesia * CD …
Contacts

Ling-Qun Hu, MD

6142936302

LingQun.Hu@osumc.edu

CONTACT

Alberto Uribe, MD

6142933559

Alberto.uribe@osumc.edu

CONTACT