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Impact of Periodontal Bacteria at Baseline on the Effectiveness of Periodontal Therapy

U

University of Messina

Status

Completed

Conditions

Periodontitis

Treatments

Procedure: Scaling and root planing

Study type

Interventional

Funder types

Other

Identifiers

NCT04382261
20-2018-10

Details and patient eligibility

About

In light of the controversy that are already approved but that however still exists regarding the efficacy and influence of the protocols for the management of Periodontitis, the aim of this study was to evaluate, at 6 months follow-up, the post-treatment clinical parameters and immunological and gingival microbial profiles in patients with periodontitis, treated by either SRP in addition to full mouth scaling or quadrant scaling

Full description

This trial was conducted in accordance with the World Medical Association's Declaration of Helsinki of 1975, and reviewed in 2008. The local ethical committee of the University of Messina approved the study protocol and each patient was carefully informed about the possible inherent risks of the study and provided their informed written consent 102 patients, , aged 27 to 65 (mean age 44.2) were assessed for eligibility. In all subjects, subgingival plaque was acquired from 4 separate proximal sites at 180 days after therapy.

Enrollment

102 patients

Sex

All

Ages

30 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. good condition of general health,
  2. a minimum of 2 teeth for each quadrant with a Pocket Depth (PD) ranging from 4-6 mm,
  3. no involvement of the furcation,
  4. a minimum of a six teeth per quadrant, respectively.

Exclusion criteria

  1. periodontal therapy during the last 12 months,
  2. assumption of antibiotics during the last 6 months,
  3. pregnancy,
  4. any systemic condition which might affect the effects of the study treatment,
  5. previous or current radiation or immunosuppressive therapies,
  6. use of mouthwash containing antimicrobials during the previous 3 months,
  7. no use of hormonal contraceptives,
  8. medication by anti-inflammatory and immunosuppressive drugs,
  9. previous history of hard-drinking,
  10. smoking,
  11. class II and III tooth mobility.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

102 participants in 2 patient groups, including a placebo group

Periodontitis quadrant
Placebo Comparator group
Description:
Patients undergo non surgical quadrant scaling and root planing
Treatment:
Procedure: Scaling and root planing
Periodontitis full mouth
Active Comparator group
Description:
Patients undergo non surgical full mouth scaling and root planing
Treatment:
Procedure: Scaling and root planing

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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