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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 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 108 other Pain, Postoperative trials with a reported enrollment target (76% lower). The trial reports 1 study location across 1 state.
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. .
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04790812
The ClinicalTrials.gov registry entry for NCT04790812 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 65 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (76% lower). The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
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 1 study location spanning 1 distinct geographic area - top geographies include 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.
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Related
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