Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02154581 · ClinicalTrials.gov registry record · NA

Case Selection and Treatment Protocol for Immediate Dental Implants in the Esthetic Zone

A NA study, sponsored by The University of Texas Health Science Center at San Antonio.

Completed
Registry status
NA
Development phase
41
Enrollment target

NCT02154581: Completed NA study, sponsored by The University of Texas Health Science Center at San Antonio.

NCT02154581 is a NA study that has completed, run by The University of Texas Health Science Center at San Antonio. The registered enrollment target is 41 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02154581, a NA study, has completed, sponsored by The University of Texas Health Science Center at San Antonio.

COMPLETED
Registry status
NA
Development phase
41 participants
Enrollment target

Study Summary

In this study a tooth that needs to be extracted will be replaced by an implant (artificial root) placed at the same appointment as the extraction. The investigators want to observe how the gums change shape with healing in two different scenarios: 1. If the soft tissue around your tooth is thin, following extraction and implant placement an extra soft tissue graft (taken from your palate) in the area in order to increase the thickness of your gums after healing. 2. If the soft tissue around your tooth is thick, the implant will be placed without a soft tissue graft. Previous studies have shown that both methods work and can give good results. In fact the two methods are used routinely but they have never been compared objectively to one another in the same research study. The main purpose of this study is to evaluate if there is any difference in terms of esthetic outcomes between these two treatment modalities after a crown has been placed on the implant.

Primary Outcome

Baseline will be at the time of crown delivery. Thereafter, the mid facial mucosal level at implant site will be recorded at 3, 6, 12 months after crown delivery.

Interventions

  • DEVICE SLActive implant

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2013-01
Est. Completion 2018-04-28
Phase NA

What the finished NCT02154581 record still lists

NCT02154581 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which SLActive implant is the first listed.

NCT02154581 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02154581 about?

NCT02154581 is a clinical study titled "Case Selection and Treatment Protocol for Immediate Dental Implants in the Esthetic Zone". In this study a tooth that needs to be extracted will be replaced by an implant (artificial root) placed at the same appointment as the extraction. The investigators want to observe how the gums change shape with healing in two different scenarios: 1. If the soft tissue around your tooth is thin, f...

What is the current status of trial NCT02154581?

This trial is currently completed. It is a NA study. The enrollment target is 41 participants. The study started on 2013-01. Estimated completion is 2018-04-28.

What interventions are being tested in trial NCT02154581?

The interventions under investigation include: SLActive implant (DEVICE).

Who is sponsoring clinical trial NCT02154581?

This trial is sponsored by The University of Texas Health Science Center at San Antonio, which has 378 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02154581's enrollment target sits among peer trials

41 1446th of 2000 higher than 554 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03449238 · 41 participants · Phase 1

    Pembrolizumab And Stereotactic Radiosurgery (Srs) Of Selected Brain Metastases In Breast Cancer Patients

  • NCT03900793 · 41 participants · Phase 1

    Losartan + Sunitinib in Treatment of Osteosarcoma

  • NCT04082520 · 41 participants · Phase 2

    Lutathera for the Treatment of Inoperable, Progressive Meningioma After External Beam Radiation Therapy

  • NCT04220190 · 41 participants · Phase 2

    RAPA-501 Therapy for ALS

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02154581, the US trial registry maintained by the National Library of Medicine. NCT02154581 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.