Comparison of Serum Trefoil Factor 3 in Patients With Gingivitis and Periodontitis After Scaling and Root Planing (CSTF3PGPSR)
Primary Purpose
Gingivitis and Periodontal Diseases
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Scaling and root planing
Sponsored by
About this trial
This is an interventional treatment trial for Gingivitis and Periodontal Diseases
Eligibility Criteria
Inclusion Criteria:
For Gingivitis:
- Gingival Index: 1.1 to 2.
- Modifies Plaque Index: 1.0 to 1.9
For Periodontitis:
- Gingival Index: 1.1 to 2.
- Modifies Plaque Index: 1.0 to 1.9
- Probing depth > 4mm
- Clinical attachment loss > 2mm
Exclusion Criteria:
For Gingivitis:
- Presence of gingival recession.
- Presence of clinical attachment loss.
- Presence of furcation.
- Presence of systemic infections like diabetes, infections.
- Smokers.
- Antibiotic therapy received preceding 3 months.
- Patients who underwent periodontal therapy within 3 months.
- Pregnant and Lactating women.
For Periodontitis:
- Presence of any systemic conditions like diabetes, infections.
- Smokers.
- Antibiotic therapy received preceding 3 months.
- Patients who underwent periodontal therapy within 3 months.
- Pregnant and Lactating women.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Experimental: Interventional
Experimental Interventional
Arm Description
Group A patients consists of Gingivitis patients whose serum is collected at base line and treated with Scaling and root planing and after three months serum is collected for assessment of Trefoil factor 3.
Group B patients consists of Periodontitis patients whose serum is collected at base line and treated with Scaling and Root Planing and after three months serum is collected for assessment of Trefoil factor 3.
Outcomes
Primary Outcome Measures
Trefoil factor 3
Blood samples were collected by venepuncture of anti-cubital vein. 2ml of blood was collected in each test tube. 10 minutes after collection, the test tube containing 2ml blood was subjected to centrifugation at 3000rpm for 10 min. The supernatant straw colored fluid (serum) was separated into storage vials (Eppendorf tubes) for serum Trefoil Factor 3.
Secondary Outcome Measures
Change in the Gingival Index.
The severity of gingivitis is scored on all surfaces of selected teeth using Williams Periodontal probe.
Index teeth- 16, 12, 24, 36, 32, 44. Score around each tooth is totalled and divided by 4-score of tooth. 0.1-1.0: Mild gingivitis. 1.1-2.0:Moderate gingivitis 2.1-3.0:Severe gingivitis
Change in Modified Plaque Index
Examination of all the surfaces of the teeth are done using an explorer. The scores for individual teeth may be grouped and totalled and divided by the number of teeth.
Excellent:0 Good:0.1-0.9 Fair:1.0-1.9 Poor:2-3
Change in Probing depth
The distance from the gingival margin to the depth of the pocket is measured using Williams periodontal probe.
Change in Clinical Attachment loss
The distance from the cementoenamel junction to the tip of the alveolar crest is measures using Williams periodontal probe.
Full Information
NCT ID
NCT03620396
First Posted
August 3, 2018
Last Updated
August 9, 2018
Sponsor
Dr.K.Sai Priyanka
Collaborators
Panineeya Mahavidyalaya Institute of Dental Sciences & Research Centre
1. Study Identification
Unique Protocol Identification Number
NCT03620396
Brief Title
Comparison of Serum Trefoil Factor 3 in Patients With Gingivitis and Periodontitis After Scaling and Root Planing
Acronym
CSTF3PGPSR
Official Title
Comparison of Serum Levels of Trefoil Factor 3 in Patients With Gingivitis and Periodontitis Following Non Surgical Periodontal Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
October 15, 2016 (Actual)
Primary Completion Date
January 17, 2017 (Actual)
Study Completion Date
February 19, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Dr.K.Sai Priyanka
Collaborators
Panineeya Mahavidyalaya Institute of Dental Sciences & Research Centre
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is intended to measure serum trefoil factor 3 at baseline and 3 months after, following nonsurgical periodontal therapy in patients with Gingivitis and Chronic Periodontitis.
Detailed Description
A goal of periodontal diagnostic procedure is to provide useful information to the clinician regarding the present periodontal disease type and severity. Advances in diagnostic research are moving towards methods where periodontal risk can be identified and quantified by objective measures such as Biomarkers.
Trefoil factors (TFFs) are one such secreted molecules derived from mucin producing epithelial cells of the gastro intestinal tracts and other tissues such as Salivary glands, Parotid ducts and oral mucosa. Among three Trefoil factors reported, Trefoil Factor 3 (TFF3) is the modifying factor for signalling pathway involved in cell survival, cell proliferation and cell migration of oral keratinocytes. Hence assessing the marker levels would achieve beneficial effects on diagnosing the disease severity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gingivitis and Periodontal Diseases
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients will be equally divided into two test groups.Group A consists of Gingivitis patients and Group B consists of Periodontitis patients. Both the group patients have been evaluated for Serum Trefoil factor 3 at baseline and treated with non surgical periodontal therapy. After three months both the group patients were again assessed for serum trefoil factor 3.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Experimental: Interventional
Arm Type
Experimental
Arm Description
Group A patients consists of Gingivitis patients whose serum is collected at base line and treated with Scaling and root planing and after three months serum is collected for assessment of Trefoil factor 3.
Arm Title
Experimental Interventional
Arm Type
Experimental
Arm Description
Group B patients consists of Periodontitis patients whose serum is collected at base line and treated with Scaling and Root Planing and after three months serum is collected for assessment of Trefoil factor 3.
Intervention Type
Procedure
Intervention Name(s)
Scaling and root planing
Intervention Description
After the serum collection is done from the patient for the assessment of trefoil factor 3, Non surgical periodontal therapy is carried out.
Primary Outcome Measure Information:
Title
Trefoil factor 3
Description
Blood samples were collected by venepuncture of anti-cubital vein. 2ml of blood was collected in each test tube. 10 minutes after collection, the test tube containing 2ml blood was subjected to centrifugation at 3000rpm for 10 min. The supernatant straw colored fluid (serum) was separated into storage vials (Eppendorf tubes) for serum Trefoil Factor 3.
Time Frame
3 months.
Secondary Outcome Measure Information:
Title
Change in the Gingival Index.
Description
The severity of gingivitis is scored on all surfaces of selected teeth using Williams Periodontal probe.
Index teeth- 16, 12, 24, 36, 32, 44. Score around each tooth is totalled and divided by 4-score of tooth. 0.1-1.0: Mild gingivitis. 1.1-2.0:Moderate gingivitis 2.1-3.0:Severe gingivitis
Time Frame
3 months
Title
Change in Modified Plaque Index
Description
Examination of all the surfaces of the teeth are done using an explorer. The scores for individual teeth may be grouped and totalled and divided by the number of teeth.
Excellent:0 Good:0.1-0.9 Fair:1.0-1.9 Poor:2-3
Time Frame
3 months
Title
Change in Probing depth
Description
The distance from the gingival margin to the depth of the pocket is measured using Williams periodontal probe.
Time Frame
3 months
Title
Change in Clinical Attachment loss
Description
The distance from the cementoenamel junction to the tip of the alveolar crest is measures using Williams periodontal probe.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
For Gingivitis:
Gingival Index: 1.1 to 2.
Modifies Plaque Index: 1.0 to 1.9
For Periodontitis:
Gingival Index: 1.1 to 2.
Modifies Plaque Index: 1.0 to 1.9
Probing depth > 4mm
Clinical attachment loss > 2mm
Exclusion Criteria:
For Gingivitis:
Presence of gingival recession.
Presence of clinical attachment loss.
Presence of furcation.
Presence of systemic infections like diabetes, infections.
Smokers.
Antibiotic therapy received preceding 3 months.
Patients who underwent periodontal therapy within 3 months.
Pregnant and Lactating women.
For Periodontitis:
Presence of any systemic conditions like diabetes, infections.
Smokers.
Antibiotic therapy received preceding 3 months.
Patients who underwent periodontal therapy within 3 months.
Pregnant and Lactating women.
12. IPD Sharing Statement
Citations:
PubMed Identifier
22181686
Citation
Chaiyarit P, Chayasadom A, Wara-Aswapati N, Hormdee D, Sittisomwong S, Nakaresisoon S, Samson MH, Pitiphat W, Giraud AS. Trefoil factors in saliva and gingival tissues of patients with chronic periodontitis. J Periodontol. 2012 Sep;83(9):1129-38. doi: 10.1902/jop.2011.110431. Epub 2011 Dec 19.
Results Reference
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PubMed Identifier
20121925
Citation
Storesund T, Schreurs O, Messelt EB, Kolltveit KM, Schenck K. Trefoil factor family 3 expression in the oral cavity. Eur J Oral Sci. 2009 Dec;117(6):636-43. doi: 10.1111/j.1600-0722.2009.00679.x.
Results Reference
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Comparison of Serum Trefoil Factor 3 in Patients With Gingivitis and Periodontitis After Scaling and Root Planing
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