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The Effect Of Biocurcumax TM Curcumin (BCM-95) In Patients With Moderate Chronic Periodontitis

The Effect Of Biocurcumax TM Curcumin (BCM-95) In Patients With Moderate Chronic Periodontitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014070918413N2
Enrollment
30
Registered
2014-08-14
Start date
2014-09-23
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: in cases for 4 weeks, two capsules(500mg) within meal will be given. Intervention 2: in the control group for 4 weeks 2 Placebo capsules with meals will be given.
Treatment - Drugs
Placebo
in cases for 4 weeks, two capsules(500mg) within meal will be given.
in the control group for 4 weeks 2 Placebo capsules with meals will be given.

Sponsors

Babol University of Medical Sience, Vice Chancellor for Research and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: In the present clinical trial study, 30 patients who are systemically healthy, but suffering from moderate chronic Periodontitis were selected. They had at least one periodontal pocket of a probe depth of 4-6 millimeters in each quadrant and bleeding during the probe. The patients who had a background of tooth scaling and root planning within the past 12 months; Exclusion criteria: those with high risk medical conditions, pregnant or breast feeding mothers, those who were cured with antibiotics or anti-inflammatory, antioxidants, or anti TNF-a within the past 6 months, as well as the presently smokers and those who have quit smoking within 1 year of the study, are not included in the research.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Gingival index. Timepoint: 0, 8 week later,4 month later. Method of measurement: the method of silness&loe,using periodontal probe.;Clinical attachment level. Timepoint: 0, 8 weeks later,4 month later. Method of measurement: with probe.;Gingival sulcus bleeding index. Timepoint: 0 ,8weeks later,4 month later. Method of measurement: after using probe,wait for 15 seconds.;Probinf pocket depth. Timepoint: 0, 8weeks later ,4 month later. Method of measurement: probe periodontal.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHedieh Ehsani

Babol University of Medical Sience

hediehehsani9@gmail.com+98 11 3222 4032

Outcome results

None listed

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