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NCT04790812 · ClinicalTrials.gov registry record · Phase 4
Preemptive Analgesia With Celecoxib for Acute Dental Pain Management
A Phase 4 study of Pain, Postoperative, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- Phase 4
- Development phase
- 65
- Enrollment target
- 1
- Study location
NCT04790812: Completed Phase 4 study of Pain, Postoperative, sponsored by The University of Texas Health Science Center, Houston.
NCT04790812 is a Phase 4 study of Pain, Postoperative that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 65 participants, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (76% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04790812, a Phase 4 study of Pain, Postoperative, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 65 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare the effect on postoperative pain of a single agent nonsteroidal anti-inflammatory drug (NSAID) \[celecoxib plus placebo\] to an NSAID combination \[celecoxib plus acetaminophen\] administered preemptively to patients prior to impacted third molar surgery. .
Primary Outcome
Psychometric response scale to be included in a questionnaire to evaluate pain intensity. A 0-10 pain scale will be used with visual "Faces" to correspond with the numerical values, with 10 indicating worse pain.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Acetaminophen
- DRUG Celecoxib
Study Locations (1)
Texas
- The University of Texas Health Science Center at Houston - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 65 participants |
| Start Date | 2021-04-22 |
| Est. Completion | 2023-03-01 |
| Phase | Phase 4 |
What the finished NCT04790812 record still lists
NCT04790812 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 participants, a relatively small participant target, below the 272-participant average among 113 other Pain, Postoperative trials with a reported enrollment target (76% lower).
The record links to 1 condition, with Pain, Postoperative appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.
NCT04790812 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT04790812 about?
NCT04790812 is a clinical study titled "Preemptive Analgesia With Celecoxib for Acute Dental Pain Management". The purpose of this study is to compare the effect on postoperative pain of a single agent nonsteroidal anti-inflammatory drug (NSAID) \[celecoxib plus placebo\] to an NSAID combination \[celecoxib plus acetaminophen\] administered preemptively to patients prior to impacted third molar surgery. .
What is the current status of trial NCT04790812?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 65 participants. The study started on 2021-04-22. Estimated completion is 2023-03-01.
What conditions does trial NCT04790812 study?
This clinical trial studies the following conditions: Pain, Postoperative.
What interventions are being tested in trial NCT04790812?
The interventions under investigation include: Placebo (DRUG), Acetaminophen (DRUG), Celecoxib (DRUG).
Who is sponsoring clinical trial NCT04790812?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04790812 being conducted?
This trial has 1 study location across Texas. 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 NCT04790812's enrollment target sits among peer trials
65 75th of 113 higher than 39 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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