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NCT03903172 · ClinicalTrials.gov registry record · NA

Post-partum Non-pharmacologic Pain Management

A NA study of Pain Management and Vaginal Delivery, sponsored by Wright State University.

Completed
Registry status
NA
Development phase
105
Enrollment target
1
Study location

NCT03903172 is a NA study of Pain Management and Vaginal Delivery that has completed, run by Wright State University. The registered enrollment target is 105 participants, below the 151-participant average among 31 other Pain Management trials with a reported enrollment target (30% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03903172, a NA study of Pain Management and Vaginal Delivery, has completed, sponsored by Wright State University.

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

Study Summary

This study aims to examine whether use of an abdominal binder for postpartum patients after vaginal delivery can effectively manage their pain and reduce the need for pharmacologic analgesics. The investigators hypothesize that use of an abdominal binder will decrease patient pain as reported on a visual analog scale of one to ten, and will decrease quantity of pain medications given. The study will be conducted at the Berry Women's Center at Miami Valley Hospital. Potential eligible participants will be approached regarding the study on admission to labor and delivery. The investigators will recruit 130 participants that will be randomized to two study arms, standard care and standard care plus abdominal binder with 65 participants in each study arm. Data will be collected prospectively while participants are admitted, and through review of electronic medical records. Potential benefits of this study include investigation of a cost-effective method for pain management that could improve patient comfort and reduce need for medications.

Interventions

  • DEVICE Abdominal binder

Study Locations (1)

Ohio

  • Miami Valley Hospital - Dayton

Trial Details

FieldValue
Enrollment Target 105 participants
Start Date 2019-06-01
Est. Completion 2024-01-31
Phase NA

Sponsor

Wright State University

32 total trials

What the Registry Record Tells You About NCT03903172

The ClinicalTrials.gov registry entry for NCT03903172 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 105 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 151-participant average among 31 other Pain Management trials with a reported enrollment target (30% lower). The listed sponsor is Wright State University, which has 32 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Pain Management appearing as the primary indexed condition, and to 1 intervention - of which Abdominal binder is the first listed.

NCT03903172 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT03903172 about?

NCT03903172 is a clinical study titled "Post-partum Non-pharmacologic Pain Management". This study aims to examine whether use of an abdominal binder for postpartum patients after vaginal delivery can effectively manage their pain and reduce the need for pharmacologic analgesics. The investigators hypothesize that use of an abdominal binder will decrease patient pain as reported on a v...

What is the current status of trial NCT03903172?

This trial is currently completed. It is a NA study. The enrollment target is 105 participants. The study started on 2019-06-01. Estimated completion is 2024-01-31.

What conditions does trial NCT03903172 study?

This clinical trial studies the following conditions: Pain Management, Vaginal Delivery.

What interventions are being tested in trial NCT03903172?

The interventions under investigation include: Abdominal binder (DEVICE).

Who is sponsoring clinical trial NCT03903172?

This trial is sponsored by Wright State University, which has 32 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03903172 being conducted?

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

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