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Clinical Trials/NCT06744348
NCT06744348
Active, not recruiting
Not Applicable

Entire Papilla Preservation Technique in the Treatment of Periodontal Intra-Bony Defects: a One-Year Clinical Follow-Up Study on Its Efficacy and Outcomes

Necmettin Erbakan University1 site in 1 country17 target enrollmentJuly 25, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Periodontal Diseases
Sponsor
Necmettin Erbakan University
Enrollment
17
Locations
1
Primary Endpoint
PROBİNG DEPTH
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

The aim of this study was to investigate the radiographic and clinical outcomes associated with the whole papilla preservation technique in the treatment of isolated intraosseous defects in patients with stage III periodontitis. The records of 17 systemically healthy patients (12 women and 5 men) diagnosed with stage III periodontitis who underwent the whole papilla preservation technique three months after nonsurgical periodontal treatment were evaluated. The following clinical parameters were recorded at baseline and after treatment: full mouth plaque score (FMPS), full mouth bleeding score (FMBS), probing depths (PD), clinical attachment level (CAL) and gingival recession (GR). The early healing index (EHI) score was assessed 1 week after surgery in both groups. CAL gain was determined as the primary outcome. Baseline data as well as follow-up assessments at 1 month, 3 months, 6 months and 1 year were analyzed to determine the efficacy and long-term outcomes of the treatment.

Registry
clinicaltrials.gov
Start Date
July 25, 2024
End Date
December 15, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Fatma Uçan Yarkaç

assoc. prof

Necmettin Erbakan University

Eligibility Criteria

Inclusion Criteria

  • • Systemically healthy individuals.
  • Patients who underwent reconstructive periodontal surgery following the completion of non-surgical treatment.
  • Presence of at least one isolated two- or three-wall intrabony defect with probing depth (PD) ≥7 mm, clinical attachment level (CAL) ≥7 mm and at least 4 mm intrabony component involving predominantly the interproximal area of the affected tooth
  • Full-mouth plaque score (FMPS) and full-mouth bleeding score ≤20%

Exclusion Criteria

  • Individuals who smoke
  • Individuals with uncontrolled systemic disease
  • Individuals using drugs that affect periodontal tissues
  • Individuals during pregnancy and breastfeeding
  • Presence of single-walled intraosseous defects
  • Flood restoration
  • Inadequate endodontic treatment

Outcomes

Primary Outcomes

PROBİNG DEPTH

Time Frame: 1 YEARS

Probing Depth (PD) refers to the distance from the gingival margin to the base of the periodontal pocket. It is expressed in mm and a high measurement is a clinically unfavorable value

Clinical Attachment Level

Time Frame: 1 YEARS

Clinical Attachment Level (CAL) is defined as the distance from the cementoenamel junction (CEJ) to the base of the periodontal pocket. It is expressed in mm and a high measurement is a clinically unfavorable value.

Study Sites (1)

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