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Evaluation of Alvora Gel in Inflammatory Factors in Patients with Periodontitis

The Effect of Topical Application of Aloe Vera Gel on IL-1B, IL-17 of Crevicular Fluid in patients with chronic Periodontitis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100412003690N11
Enrollment
34
Registered
2020-02-06
Start date
2020-02-20
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Periodontitis. Chronic periodontitis

Interventions

Intervention 1: Intervention group:Aloe vera gel will be injected into the periodontal envelope using an insulin syringe so that the gel enters and fills up to the apical envelope and the gel exits th

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 50 Years

Inclusion criteria

Inclusion criteria: Moderate to severe ?chronic periodontitis Age 35-50 Have at least 4 teeth with probe depth of 4 mm or more in each jaw quadrant Consent to participate in the study Patients candidate for non-surgical treatment

Exclusion criteria

Exclusion criteria: Allergy to aloe vera or its products Use of tobacco Endodontic and periodontal compound lesions Periapical lesions Pregnancy Severe dental caries Semi-impacted teeth Orthodontic patients Systemic diseases and systemic or topical antibiotic users 6 Months befor study Patients with periodontal disease during the past 6 months and patients receiving periodontal treatment 6 months before study Patients receiving NSAIDs one month before sampling

Design outcomes

Primary

MeasureTime frame
Plaque Index (PI). Timepoint: Before entrance in the study and 30 days after initial treatment. Method of measurement: Using the index (O'Leary 1972).;Gingival Index (GI). Timepoint: Before entrance in the study and 30 days after initial treatment. Method of measurement: According to the Loe & Sillness Index.;Probe depth (PD). Timepoint: Before entrance in the study and 30 days after initial treatment. Method of measurement: Using Williams probe 6 levels of teeth.;IL-1B. Timepoint: Before entrance in the study and 30 days after initial treatment. Method of measurement: Using ELISA kit.;IL-17. Timepoint: Before entrance in the study and 30 days after initial treatment. Method of measurement: Using ELISA kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoomeh Faramarzi

Tabriz University of Medical Sciences

?Faramarzim@tbzmed.ac.ir+98 41 1385 4863

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 10, 2026