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Clinical Trials/NCT06055686
NCT06055686
Not yet recruiting
Not Applicable

The Use of Electrical Stimulation for Determination of Epidural Catheter Placement

Stanford University1 site in 1 country50 target enrollmentNovember 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obstetric Pain
Sponsor
Stanford University
Enrollment
50
Locations
1
Primary Endpoint
Incidence rate of sacral stimulation
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

The aim of this study is to address the problem of epidural failure. The investigators theorize epidural failure can be due to inappropriate catheter movement and this may be related to the length of which the epidural catheter is inserted. The investigators will use electrical stimulation to determine if the catheter moved in the sacral direction with insertion.

Detailed Description

The research participants will be pregnant women in Labor and Delivery ward of Stanford University hospital who request an epidural for labor analgesia. In this study the patients will receive an epidural catheter in the same way as standard of care. The catheter will be inserted to 20cm and then electrically stimulated to document where it is placed by looking at the muscles effected. The catheter is then pulled back in 5cm increments and stimulated until the standard distance is achieved. For example, if loss of resistance happened at 5cm, the catheter would be inserted to 20cm, stimulated, pulled back to 15cm and stimulated, and finally to 10cm and stimulated. Electrical stimulation of epidural catheters for confirmation of placement is a published and accepted technique. In this study, the investigators will perform electrical stimulation at incremental points during catheter pull back with documentation of where stimulation was seen.

Registry
clinicaltrials.gov
Start Date
November 2025
End Date
November 2026
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Chi-Ho Ban Tsui

Professor-Med Ctr Line

Stanford University

Eligibility Criteria

Inclusion Criteria

  • Pregnant female requesting epidural for labor analgesia.
  • Must meet standard inclusion criteria for safe epidural placement.
  • Platelet count over 70,000, INR under 1.3.

Exclusion Criteria

  • Unable to safely place epidural catheter due to commonly accepted patient factors.

Outcomes

Primary Outcomes

Incidence rate of sacral stimulation

Time Frame: 1 year

Electrical stimulation will be performed at incremental points during catheter pull back with documentation of where stimulation was seen.

Study Sites (1)

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