Skip to content

Kermanshahi oil effect in treatment of gingival inflammation

Studying the effect of Kermanshahi oil gel in treatment of chronic periodontitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015122225649N1
Enrollment
20
Registered
2016-03-04
Start date
2015-11-22
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

chronic periodontitis. chronic periodontitis

Interventions

Intervention 1: intervention group 1: CHX gel ,0.5cc. Intervention 2: intervention group 2 kermanshahi oil gel ,0.5 cc. Intervention 3: control group scaling and root planning.
Treatment - Drugs
Treatment - Other
intervention group 1: CHX gel ,0.5cc
intervention group 2 kermanshahi oil gel ,0.5 cc
control group scaling and root planning

Sponsors

Ethics committee of Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Good general health with no history of any systemic disease, No history of periodontal treatment during the last six month, No history of antibiotic therapy during 3 to 4 weeks before the study begins, No history of using mouthwash during the last 2 month;Exclusion criteria: Smokers , Pregnant or lactating females

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pocket depth. Timepoint: screen day,two weeks after intervention,thirty days after intervention,forty five days after intervention. Method of measurement: measuring the distance of pocket base to the gingval margin with periodontal probe.;CAL. Timepoint: screen day,two weeks after intervention,thirty days after intervention,forty five days after intervention. Method of measurement: measuring the distance of base of the pocket from CEJ.;Gingival index. Timepoint: screen day,two weeks after intervention,thirty days after intervention,forty five days after intervention. Method of measurement: to evaluate conditions before and after phase one or surgical treatment.;Plaque index. Timepoint: screen day,two weeks after intervention,thirty days after intervention,forty five days after intervention. Method of measurement: colored surfaces of tooth by disclosing agent.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Masoome Eivazi

Kermanshah Dentistry School

m.eivazi@kums.ac.ir+98 83 3722 2400

Outcome results

None listed

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