Timing of Orthodontic Therapy and Regenerative Periodontal Surgery in Advanced Periodontitis Patients With Pathologic Tooth Migration

March 27, 2023 updated by: Karin Jepsen, University of Bonn

The Effect of Timing of Orthodontic Therapy on the Outcomes of Regenerative Periodontal Surgery in Patients With Advanced Periodontitis and Pathologic Tooth Migration. A Multi Centre Randomized Clinical Trial.

Pathologic tooth migration (PTM) is a common complication of advanced periodontitis and often motivation for patients to seek orthodontic therapy. An interdisciplinary approach is required to control the periodontal infection, reconstruct the defects and realign the migrated teeth. The optimal timing of active orthodontics after regenerative therapy is a topic of ongoing debate.

There are no data available from RCTs that have compared the effect of the timing of orthodontic tooth movement (early vs. late) on the outcomes of regenerative periodontal surgery in these patients.

It is the aim of the present randomized clinical multicenter trial to compare 2 different treatment protocols of a combined perio-regenerative and orthodontic therapy in advanced periodontitis patients with intrabony defects and pathologic tooth migration in order to establish whether one treatment modality is superior to the other with regard to clinical outcomes. A total of 46 patients will be enrolled and randomized into 2 treatment groups that differ by the time point of initiation of orthodontic therapy (early: 4 weeks vs. late: 6 months following regenerative periodontal surgery).

Primary outcome measure will be the change in clinical attachment level (CAL gain) at 12 months after regenerative therapy. Secondary outcomes will include changes in probing depth BOP, gingival recession, radiographic bone height and patient-centered outcomes.

Study Overview

Study Type

Interventional

Enrollment (Actual)

44

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • North Rhine-Westphalia
      • Bonn, North Rhine-Westphalia, Germany, 53111
        • Poliklinik für Parodontologie, Zahnerhaltung und Präventive Zahnheilkunde
      • Madrid, Spain, 28040
        • Master de Periodoncia Universidad Complutense

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Advanced periodontitis
  • Presence of intrabony defects at a minimum of 2 and a maximum of 7 adjacent teeth (positions 15-25 or 35-45) in either the maxilla or the mandible with PPD of ≥6 mm at a minimum on one site
  • Pathologic tooth migration
  • Full mouth plaque index (PI) <25% at baseline (after initial non-surgical periodontal therapy)
  • Full mouth bleeding on probing (FMBP) <25% at baseline (i.e., following initial non-surgical periodontal therapy)
  • Committed to the study and the required follow-up visits

Exclusion Criteria:

Any contraindications for oral surgical procedures

  • Uncontrolled diabetes or other uncontrolled systemic diseases
  • Disorders or treatments that compromise wound healing
  • Medical conditions requiring chronic high dose steroid therapy
  • Bone metabolic diseases
  • Radiation or other immuno-suppressive therapy
  • Infections or vascular impairment at the surgical site
  • Presence of oral lesions (such as ulceration, malignancy) or mucosal diseases
  • History of malignant disease in the oral cavity or previous radiotherapy to the head
  • Inadequate oral hygiene or unmotivated for adequate home care
  • Current smokers > 6Cig

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: ParS+Ortho 4W
Orthodontic alignment starts 4 weeks post surgical
Orthodontics 4 weeks post surgical
Active Comparator: ParS+Ortho 6M
Orthodontic alignment starts 6 months post surgical
Orthodontics 6 months post surgical

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinical attachment level (CAL) at test site
Time Frame: 12 months
Clinical attachment level (CAL)measurements 12 months after surgery
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Probing depth (PD) at test site
Time Frame: 24 months
Probing depth (PD) )measurements 12 and 24 months after surgery
24 months
Mean probing depth (PD)
Time Frame: 24 months
Mean probing depth (PD) )measurements 12 and 24 months after surgery
24 months
Bleeding on Probing (BoP) at test site
Time Frame: 24 months
Bleeding on Probing (BoP) measurements 12 and 24 months after surgery
24 months
Mean bleeding on Probing (BoP)
Time Frame: 24 months
Mean Bleeding on Probing (BoP) measurements 12 and 24 months after surgery
24 months
Plaque (PI) at test site
Time Frame: 24 months
Plaque (PI) measurements 12 and 24 months after surgery
24 months
Mean Plaque (PI)
Time Frame: 24 months
Plaque (PI) measurements 12 months after surgery
24 months
Mean clinical attachment level (CAL)
Time Frame: 24 months
Mean clinical attachment level (CAL)12 months after surgery
24 months
PROMS
Time Frame: 24 months
Patient reported Outcomes
24 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Søren Jepsen, Phd, Director
  • Principal Investigator: Karin Jepsen, Dr, OA
  • Study Chair: Andreas Jaeger, Phd, Director
  • Study Chair: Conchita Martin, PhD, Faculty of Odontology, UCM
  • Study Chair: Mariano Sanz, PhD, Faculty of Odontology, UCM

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2016

Primary Completion (Actual)

July 22, 2020

Study Completion (Actual)

March 22, 2023

Study Registration Dates

First Submitted

April 30, 2016

First Submitted That Met QC Criteria

May 1, 2016

First Posted (Estimate)

May 4, 2016

Study Record Updates

Last Update Posted (Actual)

March 30, 2023

Last Update Submitted That Met QC Criteria

March 27, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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