Effect of Probiotic in treatment of peri--implantitis

Evaluation of the effect of topical administration (mouthwash) of capsuls containing probiotics in the treatment of patients with pre-implantitis (clinical trial)

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190101042195N1

Enrollment

Registered

2020-10-28

Start date

2020-09-10

Completion date

Unknown

Last updated

2020-11-30

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

Conditions

Peri-implantitis. Diseases of oral cavity, salivary glands and jaws, Periodontal disease, , unspecified

Interventions

Intervention 1: Intervention group: Patients are scaled and given capsules of a pre-coded form (for two weeks and once a day). The intervention group is given 14 capsules containing probiotics, brand

Eligibility

Sex/Gender

All

Age

30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age 30-60 years Preimplantitis index Do not allergy to probiotics

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Measure the depth of the pocket around the implant. Timepoint: Measure the depth of the pocket at the beginning of the study and 14,30 days after the start of probiotic use. Method of measurement: probe.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaser Sargolzaei

Mashhad University of Medical Sciences

sargolzaein@mums.ac.ir+98 51 3806 7000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026