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LYZOX/Decanoic Acid (D-LYZOX)-containing Gel for Improvement of Gingivitis

Crossover Study of LYZOX/Decanoic Acid (D-LYZOX)-containing Gel for Improvement of Gingivitis - Crossover Study of D-LYZOX-containing Gel for Improvement of Gingivitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056636
Enrollment
20
Registered
2025-01-10
Start date
2025-02-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Oral disease

Interventions

Group A will use LYZOX/D-LYZOX with Decanoic Acid first. Washout period, a two-week period during which the subjects will use their regular toothpaste. Group B will use LYZOX/D-LYZOX without decanoat

Sponsors

Kanagawa Dental University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: moderate to severe periodontal disease patients without 1 type allergy

Exclusion criteria

Exclusion criteria: No periodontal disease; history of type 1 allergy.

Design outcomes

Primary

MeasureTime frame
Evaluation Period and Usage -The period of use of each D-LYZOX is usually 2 weeks, and evaluation is conducted before and after use. -Twice a day, upon waking and before bedtime, 0.2 g of D-LYZOX gel per jaw will be applied to the designated toothbrush and the patient will brush his/her teeth for 5 minutes. Assessment Items and Data Collection -Endpoints: PISA

Secondary

MeasureTime frame
Assessment Items and Data Collection -Evaluation items: PESA, PPD, CAL, BOP, Plaque Control Recode

Countries

Japan

Contacts

Public Contactkeiichi tsukinoki

Kanagawa Dental University school of Dentistry

tsukinoki@kdu.ac.jp0468228866

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026