Locally Delivered Metformin and Aloe Vera for Treatment of Intrabody Defects in Chronic Periodontitis

Sponsor
Government Dental College and Research Institute, Bangalore (Other)
Overall Status
Completed
CT.gov ID
NCT03204071
Collaborator
(none)
90
3
12

Study Details

Study Description

Brief Summary

Metformin (MF), a biguanide group of anti-diabetic drug has been shown to enhance osteoblasts differentiation and inhibit osteoclast differentiation in vitro, thus may exhibit a favorable effect on alveolar bone.

AloeVera Gel had also been used in dentistry and showed good results.The present study aims to explore the efficacy of 1% MF gel and aloe vera gel as a local drug delivery system in adjunct to scaling and root planing (SRP) for the treatment of subjects with chronic periodontitis (CP) with intrabody defects.

Condition or Disease Intervention/Treatment Phase
Phase 2/Phase 3

Detailed Description

Aim: To compare the efficacy of locally delivered 1% MF gel and aloe vera gel in treatment of intrabony defects in chronic periodontitis subjects and compare it with placebo gel.

Methods: Ninety subjects were categorized into three treatment groups: Placebo, aloevera gel(AV) and 1% Metformin (MF)after Scaling and root planning (SRP). Clinical parameters were recorded at baseline, 6 and 12 months; they included plaque index (PI), modified sulcus bleeding index (mSBI), pocket probing depth (PPD), and clinical attachment level (CAL). Radiologic assessment of intra-bony defect (IBD) and percentage defect depth reduction (DDR%) was done at baseline, 6 months and 12 months interval using computer-aided software Results: Mean PPD reduction and mean CAL gain was found to greater in MF group than AV and placebo group at all visits. The DDR% was greater in MF group as compared to AV and placebo group.

Conclusion: There was a greater decrease in mSBI and PPD and more CAL gain at the sites treated with AV and MF as an adjunct to SRP in chronic periodontitis subjects with intrabony defects as compared to placebo. The significant IBD depth reduction effect was seen in case of MFgroup.

Study Design

Study Type:
Interventional
Actual Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
COMPARATIVE EVALUATION OF SUBGINGIVALLY DELIVERED 1% METFORMIN AND ALOE VERA GEL IN TREATMENT OF INTRABODY DEFECTS IN CHRONIC PERIODONTITIS SUBJECTS: A RANDOMIZED CONTROLLED CLINICAL TRIAL
Actual Study Start Date :
Feb 1, 2016
Actual Primary Completion Date :
Feb 1, 2017
Actual Study Completion Date :
Feb 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Group 1

Placebo gel without active ingredient to be delivered at baseline, 6 and 12 months.

Drug: placebo gel
Oral prophylaxis followed by Placebo gel to be delivered in intrabody sites of chronic periodontitis subjects.
Other Names:
  • inactive drug
  • Active Comparator: Group 2

    Aloe vera gel to be delivered at baseline, 6 and 12 months.

    Drug: Aloevera
    Oral prophylaxis followed by placement of aloevera gel
    Other Names:
  • AV
  • Active Comparator: Group 3

    1% metformin gel to be delivered at baseline, 6 and 12 months.

    Drug: Metformin
    Oral prophylaxis followed by placement of metformin gel
    Other Names:
  • MF
  • Outcome Measures

    Primary Outcome Measures

    1. Change in Bone defect fill [baseline - 6 months & baseline -12 months]

      Assessed in percentage

    Secondary Outcome Measures

    1. Change in modified sulcus bleeding index [baseline, 6 & 12 months]

      scale 0-3

    2. Change in Plaque index [baseline, 6 & 12 months]

      scale 0-3

    3. Change in pocket probing depth [baseline, 6 & 12 months]

      measured in mm

    4. Clinical attachment level [baseline, 6 & 12 months]

      measured in mm

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    25 Years to 50 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    Systemically healthy patients with sites showing PPD ≥ 5 mm, CAL ≥ 4 mm and vertical bone loss ≥ 3 mm on intraoral periapical radiographs, with no history of periodontal therapy in the last 6 months.

    -

    Exclusion Criteria:
    • Subjects allergic to MF or AV Those on systemic MF or AV therapy Subjects with aggressive periodontitis Immunocompromised subjects Use of tobacco in any form, alcoholics Lactating, and pregnant females

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Government Dental College and Research Institute, Bangalore

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Dr. A R Pradeep, professor, Government Dental College and Research Institute, Bangalore
    ClinicalTrials.gov Identifier:
    NCT03204071
    Other Study ID Numbers:
    • GDCRI/ACM/PG/PhD/2/2015-2016IG
    First Posted:
    Jun 29, 2017
    Last Update Posted:
    Jun 29, 2017
    Last Verified:
    Jun 1, 2017
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 29, 2017