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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: Completed NA study of Pain Management and Vaginal Delivery, sponsored by Wright State University.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Pain score (standard scale is 0 - no pain to 10- severe pain) will be recorded by nursing staff in electronic medical record per standard of care. Average pain score for postpartum day 0 and postpartum day 1 will be computed. High scores represent greater pain.
Conditions Studied
Interventions
- DEVICE Abdominal binder
Study Locations (1)
Ohio
- Miami Valley Hospital - Dayton
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 105 participants |
| Start Date | 2019-06-01 |
| Est. Completion | 2024-01-31 |
| Phase | NA |
What the finished NCT03903172 record still lists
NCT03903172 is an interventional study that assigns participants to a tested intervention. The registered 105 participants enrollment target is mid-sized for trials with a published cap, below the 151-participant average among 31 other Pain Management trials with a reported enrollment target (30% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
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Where NCT03903172's enrollment target sits among peer trials
105 16th of 31 higher than 16 of 31 other Pain Management trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain Management 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.
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