Changes in Velocimetric Indices of Uterine and Umbilical Arteries Before and After Combined Spinal-epidural Analgesia in Laboring Women (PART II)
Recruiting
N/A
Interventional Study
Labor Pain
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.
At a Glance
- Age
- 18 – 50
- Sex
- Female
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 54 (estimated)
- Sponsor
- Samuel Lunenfeld Research Institute, Mount Sinai Hospital · Other
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About This Trial
Combined spinal-epidural (CSE) for labor analgesia has been used for many years and is practiced commonly at our institution, especially when the patient requests immediate pain relief. CSE is not only beneficial for its faster onset of analgesia, but also it is favorable in relation to the need for rescue analgesia, urinary retention, and rate of instrumental delivery compared to the traditional …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Written informed consent
* Term pregnant patients requesting labor analgesia
* Singleton pregnancy
* Term pregnant patients in active labor
* ASA\<4
* No evidence of fetal congenital anomalies, fetal compromise or fetal decelerations prior to CSE
* Patients with and without di…
Contacts