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.
Ready to participate?

Review the details below, then apply to join this clinical trial.

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
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
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
Loading…

Loading trial locations…

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

Mrinalini Balki, MD

416-586-4800

mrinalini.balki@uhn.ca

CONTACT