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NCT03022526 · ClinicalTrials.gov registry record · NA

CSE v. Epidural for Postpartum Depression

A NA study of Depression, Postpartum and Labor Pain, sponsored by Grace Lim, MD, MS.

Completed
Registry status
NA
Development phase
61
Enrollment target
1
Study location

NCT03022526 is a NA study of Depression, Postpartum and Labor Pain that has completed, run by Grace Lim, MD, MS. The registered enrollment target is 61 participants, below the 160-participant average among 15 other Depression, Postpartum trials with a reported enrollment target (62% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03022526, a NA study of Depression, Postpartum and Labor Pain, has completed, sponsored by Grace Lim, MD, MS.

COMPLETED
Registry status
NA
Development phase
61 participants
Enrollment target
1
Study location

Study Summary

The purpose of this pilot prospective randomized control trial is to compare the initiation of labor epidural analgesia by combined spinal epidural vs. epidural for the influence on risk for postpartum depression symptoms. Investigators will randomize women to the receipt of CSE or E during labor, after measuring baseline psychological, psychosocial, and psychophysical factors related to pain and depression. The immediate research goals are to understand whether the association between labor pain and PPD is modifiable through the use of tailored anesthetic techniques.

Conditions Studied

Depression, Postpartum Labor Pain

Interventions

  • PROCEDURE CSE
  • PROCEDURE Epidural
  • DRUG Bupivacaine / fentaNYL

Study Locations (1)

Pennsylvania

  • Magee Womens Hospital of UPMC - Pittsburgh

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2017-01
Est. Completion 2019-12-31
Phase NA

Sponsor

Grace Lim, MD, MS

10 total trials

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What the Registry Record Tells You About NCT03022526

The ClinicalTrials.gov registry entry for NCT03022526 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 61 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 160-participant average among 15 other Depression, Postpartum trials with a reported enrollment target (62% lower). The listed sponsor is Grace Lim, MD, MS, which has 10 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Depression, Postpartum appearing as the primary indexed condition, and to 3 interventions - of which CSE is the first listed.

NCT03022526 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT03022526 about?

NCT03022526 is a clinical study titled "CSE v. Epidural for Postpartum Depression". The purpose of this pilot prospective randomized control trial is to compare the initiation of labor epidural analgesia by combined spinal epidural vs. epidural for the influence on risk for postpartum depression symptoms. Investigators will randomize women to the receipt of CSE or E during labor, a...

What is the current status of trial NCT03022526?

This trial is currently completed. It is a NA study. The enrollment target is 61 participants. The study started on 2017-01. Estimated completion is 2019-12-31.

What conditions does trial NCT03022526 study?

This clinical trial studies the following conditions: Depression, Postpartum, Labor Pain.

What interventions are being tested in trial NCT03022526?

The interventions under investigation include: CSE (PROCEDURE), Epidural (PROCEDURE), Bupivacaine / fentaNYL (DRUG).

Who is sponsoring clinical trial NCT03022526?

This trial is sponsored by Grace Lim, MD, MS, which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03022526 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.