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The Use of Electrical Stimulation for Determination of Epidural Catheter Placement

The Use of Electrical Stimulation for Determination of Epidural Catheter Placement

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06055686
Enrollment
50
Registered
2023-09-28
Start date
2025-11-30
Completion date
2026-11-30
Last updated
2025-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, Local, Obstetric Pain

Keywords

Electrical Epidural Stimulation Test, Epidural Failure

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.

Interventions

DIAGNOSTIC_TESTElectrical Epidural Stimulation Test

Electrical stimulation test measures sensory/motor responses

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Incidence rate of sacral stimulation1 yearElectrical stimulation will be performed at incremental points during catheter pull back with documentation of where stimulation was seen.

Countries

United States

Contacts

Primary ContactKsenia Kasimova, MD
kasimova@stanford.edu6507889458

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026