Clinical evaluation of a perio gel to be used as an adjunct therapy to standard routine scaling in patients with moderate to severe periodontal disease

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

DRKS

Registry ID

DRKS00011229

Enrollment

Registered

2016-11-04

Start date

2016-09-09

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Periodontal disease K05.6

Interventions

Group 1: standard routine scaling at baseline (in-office treatment) Group 2: standard routine scaling with adjunct perio gel treatment at baseline (in-office treatment)

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: signed informed consent form; male/female; good general health, periodontal conditions

Exclusion criteria

Exclusion criteria: orthodontics applicances; tumors; participation in any other trial; pregnant/lactating women

Design outcomes

Primary

Measure	Time frame
change in periodontal attachement level at 6 months. The attachment level is determined by measuring the distance between the pocket depth and a fixed reference point on the tooth (cemento-enamel junction).	—

Secondary

Measure	Time frame
over time change in pocket depth, bleeding probing, and plaque	—

Countries

Italy, United Kingdom

Contacts

Public ContactPhilip Preshaw

University of Newcastle

philip.preshaw@newcastle.ac.uk0044-191-282-1170

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 15, 2026