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.
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