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Effect of herbal medicine, Resveratrol, on gingival infection

Comparing the effect of Resveratrol supplementation and standard treatment on clinical parameters and inflammatory markers in the patients with chronic periodontitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171015036782N6
Enrollment
40
Registered
2018-10-07
Start date
2018-04-09
Completion date
Unknown
Last updated
2018-11-05

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

Conditions

moderate to severe chronic periodontitis. Chronic periodontitis

Interventions

Intervention 1: Intervention group: Non-surgical periodontal treatment and daily administration of resveratrol 480 mg capsule, produced by Herbafit company (Germany) for 4 weeks. Intervention 2: Contr

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: age between 30 to 60 years old chronic moderate to severe periodontitis

Exclusion criteria

Exclusion criteria: Pregnancy Breast feeding Traveling for more than 2 weeks Smoking Using immunosuppressive medications Using NSAIDs Using anti hypertension drugs or Medications that slow blood clotting such as warfarin Using insulin Affecting by uterine cancer, breast cancer or ovarian cancer or being under cancer treatment Advanced kidney and liver problems Allergy to black grapes or blueberry Periodontal treatment history during the past 6 months Considerable changes in diet over the past 6 months

Design outcomes

Primary

MeasureTime frame
Probing depth. Timepoint: Beggining of study and 1 month later. Method of measurement: Williams probe.;Clinical Attachment Loss. Timepoint: Beggining of study and 1 month later. Method of measurement: Using the Williams probe.;Plaque Index. Timepoint: Beggining of study and 1 month later. Method of measurement: By colloring with disclosing pills and calculating the percentage of whole mouth.;Bleeding Index. Timepoint: Beggining of study and 1 month later. Method of measurement: Checking Bleeding on probing in the mouth and measuring its percentage.;The level of IL-8 in saliva. Timepoint: Beggining of study and 1 month later. Method of measurement: Eliza kit.;The level of IL-1ß in saliva. Timepoint: Beggining of study and 1 month later. Method of measurement: Eliza kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShabnam Nikniaz

Yazd University of Medical Sciences

sh.nikniaz@gmail.com+98 914 490 1929

Outcome results

None listed

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