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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03722446
Other study ID # 00143333
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 16, 2018
Est. completion date September 21, 2019

Study information

Verified date September 2020
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to assess if there is a difference in ability to thread the epidural catheter from two different epidural pain management kits vendors


Description:

The aim of the study is to assess if there is a difference in ability to thread the epidural catheter from two different pain management kits. In order to improve patient care, if there is a difference in the time to thread epidurals with one kit over the other, we would like to use the kit with decreased time to thread in the future.


Recruitment information / eligibility

Status Completed
Enrollment 257
Est. completion date September 21, 2019
Est. primary completion date September 21, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: women in labor

-

Exclusion Criteria:

- none

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Arrow Catheter Kit.
The group will be randomized to receive this labor analgesia kit.
B.Braun Catheter Kit
The group will be randomized to receive this labor analgesia kit.

Locations

Country Name City State
United States von Voitlander Women's Hospital Ann Arbor Michigan

Sponsors (1)

Lead Sponsor Collaborator
University of Michigan

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants Who Experienced a Successful Thread at First Pass A thread is considered successful at first pass if there were no minor or major manipulations required. within 60min of first attempt at placement
Secondary Time to Thread Epidural Catheter At the epidural placement, total amount of time required to establish successful epidural catheter thread within 60min of first attempt at placement
Secondary Incidence of Unintended Dural Punctures Count of participants for whom there was an unintended dural puncture after placement within 60min of first attempt at placement
Secondary Incidence of Paresthesia Count of participants for whom there was an incidence of paresthesia within 60min of first attempt at placement
Secondary Incidence of Epidural Intravascular Cannulations Count of participants for whom there was an incidence of epidural intravascular cannulation within 60min of first attempt at placement
Secondary Epidural Needle Manipulations Needed to Successfully Advance For each participant, the number of total manipulations (major or minor) needed to successfully advance catheter within 60min of first attempt at placement
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