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COMPLETED NA

Efficacy of EXPAREL in Comparison to Standard of Care for the Treatment of Post Operative Dental Implant Pain

NCT02533440 · View on ClinicalTrials.gov ↗

Study Summary

This study is researching managing postsurgical pain by injecting both short-acting local anesthetics and EXPAREL® at the time of surgery and reviewing if it could reduce or eliminate the need for postsurgical opioids and improve clinical outcomes following the FAST dental implant surgery procedure. This approach is being compared to the current standard of care.

Conditions Studied

Interventions

  • PROCEDURE EXPAREL and Local Anesthetics
  • PROCEDURE Oral Opioid and Local Anesthetics

Study Locations (3)

Texas

  • ClearChoice Dental Implants — Houston
  • ClearChoice Dental Implants — The Woodlands

Georgia

  • ClearChoice Dental Implants — Atlanta

Trial Details

FieldValue
Enrollment Target 69 participants
Start Date 2015-08
Est. Completion 2016-04
Phase NA

Sponsor

Bellaire Facial Surgery Center

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02533440

The ClinicalTrials.gov registry entry for NCT02533440 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 69 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bellaire Facial Surgery Center, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions — of which EXPAREL and Local Anesthetics is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02533440 reports 3 study locations spanning 2 distinct geographic areas — top geographies include Texas, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02533440 about?

NCT02533440 is a clinical study titled "Efficacy of EXPAREL in Comparison to Standard of Care for the Treatment of Post Operative Dental Implant Pain". This study is researching managing postsurgical pain by injecting both short-acting local anesthetics and EXPAREL® at the time of surgery and reviewing if it could reduce or eliminate the need for postsurgical opioids and improve clinical outcomes following the FAST dental implant surgery procedure....

What is the current status of trial NCT02533440?

This trial is currently completed. It is a NA study. The enrollment target is 69 participants. The study started on 2015-08. Estimated completion is 2016-04.

What conditions does trial NCT02533440 study?

This clinical trial studies the following conditions: Postoperative Pain. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02533440?

The interventions under investigation include: EXPAREL and Local Anesthetics (PROCEDURE), Oral Opioid and Local Anesthetics (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02533440?

This trial is sponsored by Bellaire Facial Surgery Center, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02533440 being conducted?

This trial has 3 study locations across Georgia, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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