Neuraxial block placement for Obesity Complicating Childbirth

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
University of Kentucky Medical Center, Lexington, KYObesity Complicating ChildbirthNeuraxial block placement - Procedure
Eligibility
18 - 50
Female
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Study Summary

This trial will study if using ultrasound to guide epidural needle placement in obese people during labor affects how long it takes or how many needle passes are needed.

Treatment Effectiveness

Study Objectives

2 Primary · 0 Secondary · Reporting Duration: Time from start of epidural procedure to placement of epidural needle, not to exceed more than1 hour

Hour 1
Number of passes to placement of neuraxial block in parturients with BMI=35-59.9
Time to placement of neuraxial block in parturients with BMI=35-59.9

Trial Safety

Trial Design

2 Treatment Groups

Palpation Group
1 of 2
Ultrasound Group
1 of 2

Active Control

Experimental Treatment

23 Total Participants · 2 Treatment Groups

Primary Treatment: Neuraxial block placement · No Placebo Group · N/A

Ultrasound Group
Procedure
Experimental Group · 1 Intervention: Neuraxial block placement · Intervention Types: Procedure
Palpation Group
Procedure
ActiveComparator Group · 1 Intervention: Neuraxial block placement · Intervention Types: Procedure
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Neuraxial block placement
2021
N/A
~30

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: time from start of epidural procedure to placement of epidural needle, not to exceed more than1 hour

Who is running the clinical trial?

University of KentuckyLead Sponsor
173 Previous Clinical Trials
225,583 Total Patients Enrolled
Regina Fragneto, MDPrincipal InvestigatorUniversity of Kentucky

Eligibility Criteria

Age 18 - 50 · Female Participants · 4 Total Inclusion Criteria

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Frequently Asked Questions

Is this clinical research currently accepting new volunteers?

"This medical trial is currently recruiting, with the first posting occurring on October 27th 2021 and last edit taking place on November 1st 2022. Data can be found about this project through clinicaltrials.gov's website." - Anonymous Online Contributor

Unverified Answer

Who is eligible for this research trial?

"This trial seeks 25 participants aged 18 to 50 with a BMI between 35 and 59.9 who are expecting a singleton birth at 37 weeks or later, that have consented to receive an epidural in the sitting position during labor, and fall within American Society of Anesthesiologists' classification level III or lower." - Anonymous Online Contributor

Unverified Answer

How many participants are presently partaking in this research?

"Affirmative. The details found on clinicaltrials.gov demonstrate that this investigation is actively enrolling participants. It was first announced on October 27th 2021 and the most recent edition of the study took place November 1st 2022, with 25 individuals needed from a single location." - Anonymous Online Contributor

Unverified Answer

Does this research endeavor accommodate participants aged 20 and older?

"The target demographic for this research consists of individuals who are under 50 years old and have reached the age of majority." - Anonymous Online Contributor

Unverified Answer
Please Note: These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.