MedTrace Logo

Esthetic Outcomes of Single Immediate Implant Placement

NCT02435706 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 39

Last updated 2019-05-03

Study results available
· View outcomes & findings →

Summary

A randomized controlled trial of 12-month duration to compare gingival margin location, buccal horizontal ridge dimensions, and interproximal crestal bone levels following two surgical approaches for immediate placement of implants in the esthetic zone: one involving flap elevation and another using a flapless protocol.

Conditions

  • Gingival Recession
  • Bone Loss, Alveolar

Interventions

PROCEDURE

Flapless immediate implant placement

Experimental group: No elevation of flap prior to immediate implant placement

PROCEDURE

Flap assisted immediate implant placement

Control group: Flap will be elevated prior to immediate implant placement

DEVICE

Implant and temporary crown

Both groups receive this intervention

Sponsors & Collaborators

Principal Investigators

  • Elena Sanz Miralles, DDS, MS, PhD · Columbia University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2016-08-09
Completion
2016-08-09

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02435706 on ClinicalTrials.gov