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The Effects of Aloe Vera Gel in Treating Patients with Periodontal Problems

Clinical Evaluation of Effects of Aloe Vera Gel Local Application As an Adjunct to Scaling and Root Planning in Patients with Chronic Periodontitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015010318054N2
Enrollment
18
Registered
2015-05-17
Start date
2013-10-23
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

Decreasing of periodontal pocket depth. Chronic periodontitis

Interventions

Intervention 1: In control group, a shot of distilled water was injected in periodontal pocket of contra-lateral quadrant. Intervention 2: After scaling and root planning, all patients were given a sh
Placebo
Treatment - Drugs
In control group, a shot of distilled water was injected in periodontal pocket of contra-lateral quadrant.
After scaling and root planning, all patients were given a shot of aloe Vera gel in one quadrant (test site) of their periodontal pockets, then the treated areas were covered with periodontal Coe-Pak.

Sponsors

Vice chancellor for research, Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with 4-5 millimeters of pocket depth in at least one tooth or one area in quadrant (maxilla or mandible) and with positive Bop test Exclusion criteria: Allergic history to Aloe Vera gel and its products; smoking habits; mouth breathing; tongue thrusting; combined endodontic and periodontal lesions; teeth with periapical lesion; severe caries and teeth with partial impaction; patients under orthodontic treatment; patients with systemic disease; systemic or local antibiotic therapy in six months prior to the study; any periodontal treatment six months prior to the study; pocket depths of more than 5 millimeters.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Alteration of periodontal pocket depth. Timepoint: Before the study and on thirthieth and ninetieth days. Method of measurement: Comparing plaque index, gingival index and probing depth in every stage of treatment.

Secondary

MeasureTime frame
Treatment of patients with chronic periodontitis. Timepoint: Clinical parameters including plaque index, gingival index, and probing depth were measured at the begining of study - before SRP - and also after thirty and ninety days in both quadrants. The changes of pocket depth, gingival index and plaque index were measured thirty and ninety days after the base line and variations of test and control sites were compared. Method of measurement: Comparing plaque index, gingival index and probing depth in every stage of treatment.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAidin Moghani

Guilan University of Medical Sciences

aidin_mgh@yahoo.com+98 21 2281 8152

Outcome results

None listed

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