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NCT05338671 · ClinicalTrials.gov registry record · Phase 4

Effect of Post-Operative Anesthetics on Post-Operative Pain in Patients Receiving Endodontic Treatment

A Phase 4 study of Post Operative Pain and Endodontic Disease, sponsored by University of Washington.

Completed
Registry status
Phase 4
Development phase
35
Enrollment target
1
Study location

NCT05338671 is a Phase 4 study of Post Operative Pain and Endodontic Disease that has completed, run by University of Washington. The registered enrollment target is 35 participants, below the 236-participant average among 56 other Post Operative Pain trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05338671, a Phase 4 study of Post Operative Pain and Endodontic Disease, has completed, sponsored by University of Washington.

COMPLETED
Registry status
Phase 4
Development phase
35 participants
Enrollment target
1
Study location

Study Summary

This study will assess the efficacy of two local anesthetics (2% lidocaine 1:100,000 epinephrine and 0.5% bupivicaine 1:200,000 epinephrine) in reducing post-operative pain in patients receiving endodontic treatment.

Interventions

  • DRUG Local anesthetic

Study Locations (1)

Washington

  • University of Washington- School of Dentistry - Seattle

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2021-09-29
Est. Completion 2024-06-01
Phase Phase 4

Sponsor

University of Washington

1,048 total trials

What the Registry Record Tells You About NCT05338671

The ClinicalTrials.gov registry entry for NCT05338671 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 35 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 236-participant average among 56 other Post Operative Pain trials with a reported enrollment target (85% lower). The listed sponsor is University of Washington, which has 1,048 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Post Operative Pain appearing as the primary indexed condition, and to 1 intervention - of which Local anesthetic is the first listed.

NCT05338671 reports 1 study location spanning 1 distinct geographic area - top geographies include Washington.

Frequently Asked Questions

What is clinical trial NCT05338671 about?

NCT05338671 is a clinical study titled "Effect of Post-Operative Anesthetics on Post-Operative Pain in Patients Receiving Endodontic Treatment". This study will assess the efficacy of two local anesthetics (2% lidocaine 1:100,000 epinephrine and 0.5% bupivicaine 1:200,000 epinephrine) in reducing post-operative pain in patients receiving endodontic treatment.

What is the current status of trial NCT05338671?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 35 participants. The study started on 2021-09-29. Estimated completion is 2024-06-01.

What conditions does trial NCT05338671 study?

This clinical trial studies the following conditions: Post Operative Pain, Endodontic Disease, Symptomatic Irreversible Pulpitis.

What interventions are being tested in trial NCT05338671?

The interventions under investigation include: Local anesthetic (DRUG).

Who is sponsoring clinical trial NCT05338671?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05338671 being conducted?

This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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