CClinicalTrials.gg
Active, not recruitingNCT07027137ANBperioUpdated Jun 18, 2025

The Influence of Local Antibiotic Therapy on the Outcomes Following Periodontal Regeneration Procedures.

An interventional study of SRP+ANB+SURG and SRP+SURG in Periodontitis and Periodontal Diseases, sponsored by Medical University of Bialystok. Active, not recruiting at 1 site in Poland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-06-18.

Sponsored by Medical University of Bialystok · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 9 months ago, but the record still lists the study as active, not recruiting.
  • Registered 5 years 10 months after the study started (first participant enrolled Aug 2019, registered Jun 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Assessmnet of the influence of local antibiotic therapy on the clinical, radiological, microbiological parameters and the inflammation mediators levels in the gingival crevicular fluid (GCF) following periodontal regeneration procedures in patients with periodontitis.

Read the detailed description

Forty generally healthy adults diagnosed with stage III periodontitis were randomly divided into two groups. In the test group, SRP was performed with the subsequent application of local antibiotics (10% doxycycline) into periodontal pockets at the site of the planned surgical intervention, while in the control group SRP was performed alone. Two weeks after, on the day of the surgical treatment, the M-MIST/MIST procedure was performed in both the test and control groups with the use of enamel matrix derivative (EMD). Clinical examination was performed before and 6 and 12 months after treatment. For radiological measurements RVG was performed. For inflammation mediators levels determination in GCF samples ELISA method will be used. For microbiological assessments Real Time PCR method will be used.

02

Conditions studied

  • Periodontitis
  • Periodontal Diseases

Keywords

  • periodontitis
  • periodontal regeneration
  • local antibiotics
03

In context

Periodontitis

1,635 studies on the registry are indexed under Periodontitis; 327 are open to participants now.

This study's enrollment of 40 is below the median of 45 across 1,191 interventional studies indexed under Periodontitis.

Browse Periodontitis studies →

Lead sponsor

Medical University of Bialystok is the lead sponsor of 68 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

-presence of an intrabony defect, with a pocket depth (PD) ≥ 6 mm and a radiological defect depth of ≥3 mm and width of ≥2 mm;

Exclusion criteria

Exclusion Criteria:

  • periodontal treatment within 3 months prior to the study;
  • antibiotic therapy within 3 months prior to the study;
  • smoking; presence of systemic diseases affecting periodontal healing, i.e.: immunosuppressive diseases, diabetes, osteoporosis, AIDS, hypertension treated with calcium channel blockers;
  • use of steroids or other immunosuppressive drugs;
  • pregnant and breastfeeding women
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
40 participants (actual)

Study arms

  • Experimental
    SRP+SURG

    In the control group (20 subjects) SRP was performed alone. After two weeks regeneration procedure was performed.

    Procedure: SRP+SURG

  • Experimental
    SRP+ANB+SURG

    The test group consisted of 20 people participants who underwent the SRP procedure with local antibiotic application into the pocket was performed. After two weeks regeneration procedure was performed.

    Drug: SRP+ANB+SURG

Interventions

  • DrugSRP+ANB+SURG

    SRP (scaling and root planing) with ANB (local antibiotic application- 10%doxycycline) and SURG (regeneration procedure according to MIST/M-MIST)

  • ProcedureSRP+SURG

    SRP (scaling and root planing) and SURG (regeneration procedure according to MIST/M-MIST)

06

What researchers measure

Primary outcomes

  1. Assessment of the influence of local antibiotic therapy on the clinical, outcomes following periodontal regeneration procedures.

    PD (Pocket Depth) reduction- measured from the gingival margin to the bottom of the sulcus (mm) CAL (Clinical Attachment Level) gain- measured from the cemento-enamel junction to the bottom of the sulcus (mm)

    Time frame: up to 12 months after treatment procedure

Secondary outcomes

  1. Assessment of the influence of local antibiotic therapy on the radiological outcomes following periodontal regeneration procedures.

    RIDW- (radiological intrabony defect width)- measured from bone crest to the root surface (mm) RIDD - (radiologial intrabony defect depth) - measured from bone crest to the bottom of the defect (mm)

    Time frame: up to 12 months after treatment procedure

07

Study locations

1 site
  • Department of Integrated Dentistry, Medical University of Białystok
    Białystok, Podlaskie 15-089, Poland
08

References and documents

Individual participant data

Plan to share: No — IPD cannot be transferred to other people due to GDPR

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07027137
Lead sponsor
Medical University of Bialystok
Responsible party
Sponsor
First posted
Jun 18, 2025
Start date
Aug 1, 2019
Primary completion
Dec 30, 2025 (estimated)
Completion
Dec 30, 2025 (estimated)
Last update
Jun 18, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion