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Iranian Traditional Mouth Rinse Punica Granatum Pleniflora (Golnaar) in Treatment of Gingivitis in Diabetic Patients (Golnaar)

Primary Purpose

Gingivitis

Status
Completed
Phase
Not Applicable
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Punica granatum Pleniflora (Golnaar) mouth rinse
Chlorhexidine (0.2%)
Tooth bleaching
Sponsored by
Shiraz University of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gingivitis focused on measuring Gingivitis, Diabetes mellitus, Medicine, Traditional, Herbal medicine, Punica granatum

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • To have gingivitis
  • Controlled diabetes mellitus [FBS<130mg/dl & Glycosilated hemoglobin (A1C)<7%]
  • Presence of gingivitis
  • Having at least 20 teeth
  • No history of hypersensitivity reaction
  • Age between 20 to 65 years
  • Agreement to participate in the study

Exclusion Criteria:

  • History of hypersensitivity reaction
  • Smoking
  • Systemic diseases (Kidney, liver or rheumatologic diseases)
  • To have a pocket depth of more than 5
  • Consumption of antibiotics, corticosteroids or nonsteroidal anti-inflammatory drugs in the past 3 months and during the study period

Sites / Locations

  • Motahhari clinic of Shiraz University of Medical Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Chlorhexidine (0.2%)

Punica granatum Pleniflora mouth rinse

Arm Description

Chlorhexidine (0.2%) mouth rinse, 10 ml for 2 minutes every night for 2 weeks and tooth bleaching (one time) after using mouth rinse.

Punica granatum Pleniflora (Golnaar) mouth rinse, 10 ml for 2 minutes every night for 2 weeks and tooth bleaching (one time) after using mouth rinse.

Outcomes

Primary Outcome Measures

Plaque Index
0 No plaque A film of plaque adhering to the free gingival margin and adjacent area of the tooth, which cannot be seen with the naked eye. But only by using disclosing solution or by using probe. Moderate accumulation of deposits within the gingival pocket, on the gingival margin and/ or adjacent tooth surface, which can be seen with the naked eye. Abundance of soft matter within the gingival pocket and/or on the tooth and gingival margin.
Bleeding Index
presence of bleeding of the gum when probing it: 0= No bleeding 1= Bleeding occurs within 10 seconds after gentle probing of the orifice of the gingival crevice
Pocket Depth
It is the depth of the dental sulcus which detected by measuring the depth of sulcular insertion of the probe at six sites; mesiofacial, midfacial, distofacial, mesiolingual, midlingual and distolingual of all teeth divided by the teeth number. the measurement unit is millimeter (mm).
Modified Gingival Index
0= Absence of inflammation Mild inflammation or with slight changes in color and texture but not in all portions of gingival marginal or papillary Mild inflammation, such as the preceding criteria, in all portions of gingival marginal or papillary moderate, bright surface inflammation, erythema, edema and/or hypertrophy of gingival marginal or papillary severe inflammation: erythema, edema and/or marginal gingival hypertrophy of the unit or spontaneous bleeding, papillary, congestion or ulceration

Secondary Outcome Measures

Number of Participants With Adverse Events
Satisfaction of Patients
We use a Visual Analogue Scale (VAS) to evaluate the patients' satisfaction and their tolerance. This "VAS" ranged from 1 (not satisfied at all) to 5 (fully satisfied) was used: Not satisfied at all Not satisfied adequately Not good-Not bad (So So) Mostly Satisfied Fully satisfied

Full Information

First Posted
August 22, 2014
Last Updated
July 13, 2016
Sponsor
Shiraz University of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02227485
Brief Title
Iranian Traditional Mouth Rinse Punica Granatum Pleniflora (Golnaar) in Treatment of Gingivitis in Diabetic Patients
Acronym
Golnaar
Official Title
Evaluation of the Effects of an Iranian Traditional Mouth Rinse Punica Granatum Pleniflora (Golnaar) in Treatment of Gingivitis in Patients With Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
July 2014 (undefined)
Primary Completion Date
November 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shiraz University of Medical Sciences

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a triple-blinded randomized clinical trial to evaluate the effect of an Iranian traditional mouth rinse (Punica granatum Pleniflora or "Golnaar" mouthrinse) on treatment of diabetic gingivitis and compare it with chlorhexidine (0.2%).
Detailed Description
Among diabetic patients who refer to Motahhari clinic of Shiraz University of Medical Sciences 80 volunteers who have gingivitis and aged between 20 to 65 years old and fulfill other inclusion criteria, are randomly assigned to intervention or control groups. All of the patients will undergo a training panel about mouth hygiene and receive a pack of a toothbrush, a toothpaste, a dental floss and a mouth rinse. They are asked to return after 2 weeks for the second evaluation and taking tooth bleaching. The demographic and general information of all participants are taken and the primary outputs (plaque index and bleeding on probe) are measured at the beginning, after 2 weeks and after 4 weeks. All the examinations are done by one trained person and patients, practitioner and statistical analyser are blind to the interventions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gingivitis
Keywords
Gingivitis, Diabetes mellitus, Medicine, Traditional, Herbal medicine, Punica granatum

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Chlorhexidine (0.2%)
Arm Type
Active Comparator
Arm Description
Chlorhexidine (0.2%) mouth rinse, 10 ml for 2 minutes every night for 2 weeks and tooth bleaching (one time) after using mouth rinse.
Arm Title
Punica granatum Pleniflora mouth rinse
Arm Type
Experimental
Arm Description
Punica granatum Pleniflora (Golnaar) mouth rinse, 10 ml for 2 minutes every night for 2 weeks and tooth bleaching (one time) after using mouth rinse.
Intervention Type
Drug
Intervention Name(s)
Punica granatum Pleniflora (Golnaar) mouth rinse
Other Intervention Name(s)
Intervention group
Intervention Description
All the patient in intervention group use 10 ml of "Golnaar" mouth rinse for 2 minutes every night for 2 weeks.
Intervention Type
Drug
Intervention Name(s)
Chlorhexidine (0.2%)
Other Intervention Name(s)
Control group
Intervention Description
All the patient in control group use 10 ml of chlorhexidine (0.2%) for 2 minutes every night for 2 weeks.
Intervention Type
Procedure
Intervention Name(s)
Tooth bleaching
Other Intervention Name(s)
Bleaching
Intervention Description
Tooth bleaching for both groups one time after using mouth rinses.
Primary Outcome Measure Information:
Title
Plaque Index
Description
0 No plaque A film of plaque adhering to the free gingival margin and adjacent area of the tooth, which cannot be seen with the naked eye. But only by using disclosing solution or by using probe. Moderate accumulation of deposits within the gingival pocket, on the gingival margin and/ or adjacent tooth surface, which can be seen with the naked eye. Abundance of soft matter within the gingival pocket and/or on the tooth and gingival margin.
Time Frame
At the beginning, after 2 weeks and after 4 weeks
Title
Bleeding Index
Description
presence of bleeding of the gum when probing it: 0= No bleeding 1= Bleeding occurs within 10 seconds after gentle probing of the orifice of the gingival crevice
Time Frame
At the beginning, after 2 weeks and after 4 weeks.
Title
Pocket Depth
Description
It is the depth of the dental sulcus which detected by measuring the depth of sulcular insertion of the probe at six sites; mesiofacial, midfacial, distofacial, mesiolingual, midlingual and distolingual of all teeth divided by the teeth number. the measurement unit is millimeter (mm).
Time Frame
At the beginning, after 2 weeks and after 4 weeks
Title
Modified Gingival Index
Description
0= Absence of inflammation Mild inflammation or with slight changes in color and texture but not in all portions of gingival marginal or papillary Mild inflammation, such as the preceding criteria, in all portions of gingival marginal or papillary moderate, bright surface inflammation, erythema, edema and/or hypertrophy of gingival marginal or papillary severe inflammation: erythema, edema and/or marginal gingival hypertrophy of the unit or spontaneous bleeding, papillary, congestion or ulceration
Time Frame
At the beginning, after 2 weeks and after 4 weeks.
Secondary Outcome Measure Information:
Title
Number of Participants With Adverse Events
Time Frame
Up to 2 weeks
Title
Satisfaction of Patients
Description
We use a Visual Analogue Scale (VAS) to evaluate the patients' satisfaction and their tolerance. This "VAS" ranged from 1 (not satisfied at all) to 5 (fully satisfied) was used: Not satisfied at all Not satisfied adequately Not good-Not bad (So So) Mostly Satisfied Fully satisfied
Time Frame
Up to 2 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: To have gingivitis Controlled diabetes mellitus [FBS<130mg/dl & Glycosilated hemoglobin (A1C)<7%] Presence of gingivitis Having at least 20 teeth No history of hypersensitivity reaction Age between 20 to 65 years Agreement to participate in the study Exclusion Criteria: History of hypersensitivity reaction Smoking Systemic diseases (Kidney, liver or rheumatologic diseases) To have a pocket depth of more than 5 Consumption of antibiotics, corticosteroids or nonsteroidal anti-inflammatory drugs in the past 3 months and during the study period
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mesbah Shams, MD
Organizational Affiliation
Research Center for Traditional Medicine & History of Medicine - Shiraz University of Medical Sciences
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mohammad Mahdi Fani, Dentist
Organizational Affiliation
Research Center for Traditional Medicine & History of Medicine-Shiraz University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Massih Seddigh-Rahimabadi, MD
Organizational Affiliation
Shiraz University of Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Motahhari clinic of Shiraz University of Medical Sciences
City
Shiraz
State/Province
Fars
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All the records have been collected and archived, and can be reused if is necessary.

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Iranian Traditional Mouth Rinse Punica Granatum Pleniflora (Golnaar) in Treatment of Gingivitis in Diabetic Patients

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