Effect of non-surgical periodontal therapy on serum level of transferrin and clinical parameters in patients with periodontal disease

Effect of non-surgical periodontal therapy on serum transferrin levels in chronic periodontitis patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201601137128N6

Enrollment

Registered

2016-04-26

Start date

2015-04-05

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Chronic periodontitis. Chronic periodontitis

Interventions

Intervention 1: Intervention: chronic periodontitis : Patients in the chronic periodontitis group received nonsurgical periodontal therapy, including oral hygiene instructions(flossing & brushi

Treatment - Other

Intervention: chronic periodontitis : Patients in the chronic periodontitis group received nonsurgical periodontal therapy, including oral hygiene instructions(flossing & brushing with Bass te

Control: healthy periodontal control group subjects were provided with oral hygiene instructions(flossing & brushing with Bass technique) only in 1 20minute session

Eligibility

Sex/Gender

All

Age

25 Years to 60 Years

Inclusion criteria

Inclusion criteria: inclusion criteria in periodontally healthy group:no evidence of interproximal attachment loss, no PD equal or more than 3mm at any sites on any teeth and whole-mouth bleeding scores equal or less than 10%. inclusion criteria in chronic periodontitis group: two or more interproximal sites with attachment loss equal or more than 4mm, or two or more interproximal sites with PD equal or more 5mm,not on same tooth. Exclusion criteria :1) a course of NSAIDs or antimicrobial drugs within a 6 month period before the study 2)history of any periodontal treatment within a 6 month period before the study 3) presence of any systemic disease and infection other than chronic periodontitis 4)presence of aggressive periodontitis 5)pregnancy or lactating mothers 6) use of mouthwashes or vitamin supplements within the previous 3 months 7) furca involvement grade 2 , 3 , 4

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

Measure	Time frame
Clinical parameters of periodontium. Timepoint: Base line-3month. Method of measurement: periodontal probing.	—

Primary

Measure	Time frame
Serum level of transferrin. Timepoint: Base line-3month. Method of measurement: laboratory test.	—

Countries

Iran (Islamic Republic of)

Contacts

Public Contactashkan salari

Tabriz university of medical science

drashkan_salari@yahoo.com+98 41 1335 5965

Outcome results

None listed

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