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The effect of non-surgical periodontal treatment on salivary and serum visfatin

The effect of non-surgical periodontal treatment on salivary and serum visfatin in generalized moderate to severe chronic periodontitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012080510501N1
Enrollment
18
Registered
2012-08-25
Start date
2012-09-22
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

generalized modorate to severe chronic periodontitis. Chronic periodontitis

Interventions

Scaling and root planning by ultrasonic and hand instruments.
Treatment - Devices
Scaling and root planning by ultrasonic and hand instruments

Sponsors

vice-chancellor for research of Tabriz university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: individuals whit BMI 18-24.9 kg/m2; natural teeth =20; GI>1; moderate to severe chronic periodontitis in which at least 30% sites have CAL=3mm and PPD=5mm and radiographic signs of bone loss are present. Exclusion criteria: individuals with systemic diseases that can alter the course of periodontal disease; pregnancy or lactation; hypertension; aggressive periodontitis; history of using anti hyperlipidemia medication or antibiotic in the preceding 6 months; ongoing usage of NSAIDs; a smoking habit; or those who had received scaling and root planning in the preceding 6 months.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum visfatin. Timepoint: before intervention, one month after intervention. Method of measurement: Eliza kit.;Salivary visfatin. Timepoint: before intervention, one month after intervention. Method of measurement: Eliza kit.

Secondary

MeasureTime frame
Gingival index. Timepoint: before intervention, one month after intervention. Method of measurement: gingival index score.;Clinical attachment level. Timepoint: before intervention, one month after intervention. Method of measurement: prob.;Clinical pocket depth. Timepoint: before intervention, one month after intervention. Method of measurement: prob.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Nader Abolfazli

Tabriz faculty of dentistry

Abolfazli@tbzmed.ac.ir+98 41 1335 5965

Outcome results

None listed

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