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NCT06495632 · ClinicalTrials.gov registry record · Phase 4
Scheduled or As Needed Pain Regimen?
A Phase 4 study of Pain, Postoperative, sponsored by Cape Fear Valley Health System.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 90
- Enrollment target
- 1
- Study location
NCT06495632: Recruiting Phase 4 study of Pain, Postoperative, sponsored by Cape Fear Valley Health System.
NCT06495632 is a Phase 4 study of Pain, Postoperative that is actively recruiting participants, run by Cape Fear Valley Health System. The registered enrollment target is 90 participants, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (67% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06495632, a Phase 4 study of Pain, Postoperative, is actively recruiting participants, sponsored by Cape Fear Valley Health System.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 90 participants
- Enrollment target
- 1
- Study location
Study Summary
The aim of this study is to determine feasibility of a randomized controlled trial and estimates of efficacy for pain control of a scheduled pain regimen versus an as needed pain regimen for participants undergoing same day surgery procedures.
Primary Outcome
To measure feasibility of the study, the following data will be collected: 1. Number of participants eligible for the study 2. Number of participants contacted about the study 3. Number of participants consented 4. Number of participants being at least 80% adherent to medication protocol 5. Number of drop-outs in the study and reason for drop out 6. Number of Adverse Events reported to study personnel. For all non-consented participants, only counts will be included (e.g., 5 participants who re
Conditions Studied
Interventions
- DRUG Motrin and narcotic
Study Locations (1)
North Carolina
- Cape Fear Valley Medical Center - Fayetteville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2024-08-01 |
| Est. Completion | 2027-07-31 |
| Phase | Phase 4 |
What NCT06495632 shows while recruiting
NCT06495632 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (67% lower).
The record links to 1 condition, with Pain, Postoperative appearing as the primary indexed condition, and to 1 intervention - of which Motrin and narcotic is the first listed.
NCT06495632 reports a single indexed study location in North Carolina.
Frequently Asked Questions
What is clinical trial NCT06495632 about?
NCT06495632 is a clinical study titled "Scheduled or As Needed Pain Regimen?". The aim of this study is to determine feasibility of a randomized controlled trial and estimates of efficacy for pain control of a scheduled pain regimen versus an as needed pain regimen for participants undergoing same day surgery procedures.
What is the current status of trial NCT06495632?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 90 participants. The study started on 2024-08-01. Estimated completion is 2027-07-31.
What conditions does trial NCT06495632 study?
This clinical trial studies the following conditions: Pain, Postoperative.
What interventions are being tested in trial NCT06495632?
The interventions under investigation include: Motrin and narcotic (DRUG).
Who is sponsoring clinical trial NCT06495632?
This trial is sponsored by Cape Fear Valley Health System, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06495632 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Pain, Postoperative
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 NCT06495632's enrollment target sits among peer trials
90 50th of 113 higher than 61 of 113 other Pain, Postoperative trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pain, Postoperative 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
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