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Study of a product containing Phtalox® for the prevention and control of Pyorrhea

Clinical study of a formulation containing Phtalox® for the prevention and control of Periodontal Disease

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
REBEC
Registry ID
RBR-6jts634
Enrollment
Unknown
Registered
2021-09-24
Start date
2022-03-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Mouthwashes

Interventions

Basic periodontal treatments will be performed on patients. After this stage, individuals will be randomly divided based on a draw with closed, opaque and non-translucent envelopes, in 3 groups accord
G2 - patients who will perform mouthwashes with 0.12% chlorhexidine and G3 - patients who will be treated with PHTALOX®. Each group will be composed of the same number of patients, that is, 10. Patien
E06.721.189.350

Sponsors

Universidade Federal de Alfenas
Lead Sponsor
Universidade Federal de Alfenas
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Individuals of both sexes; no history of systemic complications for more than 6 months; no recent drug history; systemically healthy; PD patients.

Exclusion criteria

Exclusion criteria: Individuals who do not wish to complete the treatment protocol; individuals with healthy periodontium; pregnancy; lactation; drug abuse; individuals with systemic changes; individuals who have used antibiotics in the past 3 months; individuals with systemic diseases requiring antibiotic prophylaxis prior to periodontal therapy; immunosuppressed individuals.

Design outcomes

Primary

MeasureTime frame
It is expected with the use of a mouthwash containing a PHTALOX® formulation as an adjunct to the treatment of scaling and root planing and maintenance of Periodontal Disease in humans, to find an improvement in the periodontal clinical parameters measured in millimeters with the periodontal probe such as level of clinical insertion, probing depth, in addition to the CPI, O 'LEARY and ISS indexes.

Secondary

MeasureTime frame
No secondary outcomes are expected.

Countries

Brazil

Contacts

Public ContactLeandro Fernandes
learaujofernandes@gmail.com+55-35-992100616

Outcome results

None listed

Source: REBEC (via WHO ICTRP)