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NCT06528574 · ClinicalTrials.gov registry record · NA
Postoperative Pain After Activation of Irrigant
A NA study of Pain, sponsored by Cleveland Dental Institute.
- Recruiting
- Registry status
- NA
- Development phase
- 84
- Enrollment target
- 1
- Study location
NCT06528574 is a NA study of Pain that is actively recruiting participants, run by Cleveland Dental Institute. The registered enrollment target is 84 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (72% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06528574, a NA study of Pain, is actively recruiting participants, sponsored by Cleveland Dental Institute.
- RECRUITING
- Registry status
- NA
- Development phase
- 84 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research is to analyze the levels of pain after cleaning and shaping in individuals who are receiving root canal therapy using the IVAC irrigation approach, and those who are treated with ultrasonic irrigation techniques, negative pressure irrigation technique and traditional irrigation techniques. PICOTS Question: Does the new Dent's iVac irrigation protocol has an effect on reduction of postoperative pain By enlisting at least 84 suitable individuals who are undergoing the identical endodontic procedure. pain will be measures by assessing pain levels through a standardized numerical rate scale (NRS) at certain time intervals after root canal treatment, 6 hours, 12 hours, 24 hours, 48 hours, and 72 hours.
Conditions Studied
Interventions
- DEVICE Conventional root canal treatment
- DEVICE Ultrasonic
- DEVICE Apical negative pressure
- DEVICE Combined Ultrasonic and negative pressure
Study Locations (1)
Ohio
- Cleveland Dental Institute - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 84 participants |
| Start Date | 2023-08-01 |
| Est. Completion | 2025-04-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06528574
The ClinicalTrials.gov registry entry for NCT06528574 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 84 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 304-participant average among 374 other Pain trials with a reported enrollment target (72% lower). The listed sponsor is Cleveland Dental Institute, which has 6 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Pain appearing as the primary indexed condition, and to 4 interventions - of which Conventional root canal treatment is the first listed.
NCT06528574 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT06528574 about?
NCT06528574 is a clinical study titled "Postoperative Pain After Activation of Irrigant". The purpose of this research is to analyze the levels of pain after cleaning and shaping in individuals who are receiving root canal therapy using the IVAC irrigation approach, and those who are treated with ultrasonic irrigation techniques, negative pressure irrigation technique and traditional irr...
What is the current status of trial NCT06528574?
This trial is currently recruiting. It is a NA study. The enrollment target is 84 participants. The study started on 2023-08-01. Estimated completion is 2025-04-30.
What conditions does trial NCT06528574 study?
This clinical trial studies the following conditions: Pain.
What interventions are being tested in trial NCT06528574?
The interventions under investigation include: Conventional root canal treatment (DEVICE), Ultrasonic (DEVICE), Apical negative pressure (DEVICE), Combined Ultrasonic and negative pressure (DEVICE).
Who is sponsoring clinical trial NCT06528574?
This trial is sponsored by Cleveland Dental Institute, which has 6 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06528574 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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