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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04633824
Other study ID # IRB-300006294
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date February 1, 2021
Est. completion date January 1, 2025

Study information

Verified date May 2024
Source University of Alabama at Birmingham
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The Agency for Healthcare Research and Quality (AHRQ) defines a disparity as a difference or a gap that exist between two groups, which is both statistically significant, larger than 10%, and indicates poor quality for the minority (non-referent) group. Despite advances in public health initiatives and medicine, disparities in healthcare are persistent. For example, in the United States, maternal mortality ratio has doubled since 1987 to 2009 where African American women were 4 times as likely to die from childbirth. Although there was no observed racial disparity in maternal deaths at University of Alabama Birmingham, there is anecdotal experience that may suggest health disparities do exist on the labor floor when examining neuraxial utilization and effectiveness. This retrospective study will seek to examine the successful extension of labor analgesia for cesarean section as it relates to insurance status.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 2500
Est. completion date January 1, 2025
Est. primary completion date November 1, 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Pregnancy - Age >/= age 18 years Exclusion Criteria: - Women less than age 18 will be excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Retrospective Electronic Medical Record Review
Patients will be assessed retrospectively for evidence of successful or failed epidural extension in the setting of need for cesarean section

Locations

Country Name City State
United States University of Alabama at Birmingham Birmingham Alabama

Sponsors (1)

Lead Sponsor Collaborator
University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Successful extension of labor epidural catheter for cesarean section labor epidural activation in the setting of cesarean section from the time of admission to the time of delivery
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