Last updated: March 13, 2025
Sponsor: Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Overall Status: Active - Recruiting
Phase
N/A
Condition
Acute Pain
Treatment
Epidural catheter
Clinical Study ID
NCT04946032
21-06
Ages 18-50 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
All women aged 18 years and above.
In established second stage of labor.
3-7 cm dilation at time of insertion.
Women with BMI < 40 kg/m2
Exclusion
Exclusion Criteria:
Known contraindication to epidural insertion.
Inability or unwillingness to provide written consent.
Previous difficult epidural insertion.
Previous failed epidural.
Imminent instrumental or operative delivery.
Dural puncture.
Combined spinal epidural analgesia.
High BMI > 40 kg/m2
Study Design
Total Participants: 200
Treatment Group(s): 1
Primary Treatment: Epidural catheter
Phase:
Study Start date:
November 23, 2021
Estimated Completion Date:
June 30, 2025
Study Description
Connect with a study center
Mount Sinai Hospital
Toronto, Ontario M5G1X5
CanadaActive - Recruiting
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