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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04399187
Other study ID # 16-18
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2018
Est. completion date September 15, 2019

Study information

Verified date May 2020
Source University of Messina
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study was to assess the efficacy of minimally invasive nonsurgical debridement (MINSD) of periodontal pockets with or without local amino acid buffered sodium hypochlorite (NaOCl) gel application after 6 months follow-up.


Description:

Forty periodontal compromised patients were randomly allocated in two groups. Periodontal pockets > 5 mm in patients of test group were treated by MINSD and NaOCl gel application, meanwhile in patients of control group MINSD alone was performed. Full-mouth plaque score (FMPS) , Full-mouth bleeding score (FMBS), probing depth (PD), clinical attachment level (CAL) and gingival recession (GR) were assessed at baseline and after 6 months follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date September 15, 2019
Est. primary completion date September 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 32 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients diagnosed with periodontitis;

- Age > 18 years old;

- Patients with at least 10 teeth for arch;

- Presence at least of two teeth with PD > 5 mm for quadrant;

- Single-rooted and multi-rooted teeth;

Exclusion Criteria:

- Patients with systemic diseases;

- Pregnant or lactating;

- Tobacco smokers (> 10 cigarettes/day);

- Previous periodontal treatment in the last 2 years;

- Prolonged antibiotic treatment or anti-inflammatory treatment within 6 months prior to periodontal therapy;

- Furcation involvement;

- Acute periodontal or endodontic abscess;

- Third molars

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Sodium hypochlorite gel application
Patients treated by scaling and root planing and Sodium hypochlorite gel application, meanwhile in patients of control group scaling and root planing alone was performed.

Locations

Country Name City State
Italy University of Messina Messina

Sponsors (1)

Lead Sponsor Collaborator
University of Messina

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Probing depth changes Changes over time in probing depth millimiters 6-months
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