Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04109365 · ClinicalTrials.gov registry record · NA

Obstetric Placement Study Using EST

A NA study of Anesthesia, Local and Obstetric Pain, sponsored by Stanford University.

Recruiting
Registry status
NA
Development phase
40
Enrollment target
1
Study location

NCT04109365: Recruiting NA study of Anesthesia, Local and Obstetric Pain, sponsored by Stanford University.

NCT04109365 is a NA study of Anesthesia, Local and Obstetric Pain that is actively recruiting participants, run by Stanford University. The registered enrollment target is 40 participants, below the 81-participant average among 18 other Anesthesia, Local trials with a reported enrollment target (51% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04109365, a NA study of Anesthesia, Local and Obstetric Pain, is actively recruiting participants, sponsored by Stanford University.

RECRUITING
Registry status
NA
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

Combined spinal-epidural (CSE) is an established technique for providing labour analgesia to obstetric patients which provides rapid onset but unsustained analgesia. The epidural catheter can be used to extend and provide continuous pain relief, however during single-segment needle-through-needle CSE, the catheter is untested. This study aims to confirm placement of epidural catheters of anesthesia through the epidural stimulation test (EST) which was first described by the PI of the study for confirming placement of epidural catheters approximately 20 years ago.

Primary Outcome

Investigate the ability of the electrical epidural stimulation test (EST) to determine the position of the epidural catheter anesthesia for labour analgesia after low-dose anesthetic as compared to the gold standard of clinical assessment.

Interventions

  • DIAGNOSTIC_TEST Electrical Epidural Stimulation Test (EST)

Study Locations (1)

California

  • Lucille Packard Children's Hospital - Palo Alto

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2020-12-15
Est. Completion 2025-12
Phase NA
Stanford University

1,744 total trials

What NCT04109365 shows while recruiting

NCT04109365 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 81-participant average among 18 other Anesthesia, Local trials with a reported enrollment target (51% lower).

The record links to 2 conditions, with Anesthesia, Local appearing as the primary indexed condition, and to 1 intervention - of which Electrical Epidural Stimulation Test (EST) is the first listed.

NCT04109365 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT04109365 about?

NCT04109365 is a clinical study titled "Obstetric Placement Study Using EST". Combined spinal-epidural (CSE) is an established technique for providing labour analgesia to obstetric patients which provides rapid onset but unsustained analgesia. The epidural catheter can be used to extend and provide continuous pain relief, however during single-segment needle-through-needle CS...

What is the current status of trial NCT04109365?

This trial is currently recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2020-12-15. Estimated completion is 2025-12.

What conditions does trial NCT04109365 study?

This clinical trial studies the following conditions: Anesthesia, Local, Obstetric Pain.

What interventions are being tested in trial NCT04109365?

The interventions under investigation include: Electrical Epidural Stimulation Test (EST) (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT04109365?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04109365 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Anesthesia, Local

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04109365's enrollment target sits among peer trials

40 12th of 18 higher than 6 of 18 other Anesthesia, Local trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Anesthesia, Local trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01306019 · 40 participants · Phase 1

    Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)

  • NCT01608152 · 40 participants

    Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors

  • NCT01668082 · 40 participants · NA

    An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection

  • NCT02015013 · 40 participants · Phase 2

    Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04109365, the US trial registry maintained by the National Library of Medicine. NCT04109365 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.