Opioid Education Ventral Hernia Repair
Public ClinicalTrials.gov record NCT07639281. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
The Effect on Educational Videos on Opioid Use
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The goal of this study is to learn if opioid education before surgery affects prescribed opioid use after surgery in participants who are undergoing a ventral hernia repair. The main question it aims to answer is, does opioid education before surgery lower the number of opioid pills taken during recovery after a ventral hernia repair? Researchers will compare participants who watch an opioid education video before surgery to participants who watch a ventral hernia repair education video before surgery to see if those who watch an opioid education video take less prescribed opioid pills during recovery. Participants will watch a roughly 2-minute video in office the day their ventral hernia repair is scheduled, watch the same video the day of their surgery and be asked to report how many prescription opioid pills they took during recovery and return any left-over prescription opioid pills for disposal at their 1 month follow up appointment.
Study identification
- NCT ID
- NCT07639281
- Recruitment status
- Enrolling by invitation
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 75 participants
Conditions and interventions
Interventions
- Opioid and Surgery Education Video Behavioral
- Surgery Education Video Behavioral
Behavioral
Eligibility (public fields only)
- Age range
- 18 Years to 85 Years
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Feb 14, 2024 (Actual)
- Primary completion
- Dec 2026 (Estimated)
- Completion
- Jan 2027 (Estimated)
- Last update posted
- Jun 10, 2026
2024 – 2027
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of Kentucky | Lexington | Kentucky | 40536 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT07639281, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jun 10, 2026 · Synced Oct 19, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT07639281 live on ClinicalTrials.gov.