Teh Effect of Subgingival Irrigation Wif Ketorolac and Chlorhexidine in Patients Wif Chronic Periodontist

NCT ID: NCT03836781

Last Updated: 2019-07-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2/PHASE3

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-04-10

Study Completion Date

2019-06-15

Brief Summary

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In this study, 40 patients with a history of Mild- Periodontitis who were diagnosed with clinical and radiographic findings showed that all of the periodontal parameters before the treatment, during the treatment period Then, scaling \& Root planing and oral hygiene instructions were given to the patients, and after 2 weeks, the patients who received the study were randomly divided into two groups (Balanced Block Randomization) with four blocks according to the visit time. To group A, oral chlorohexidine and to B group, the drug Ketorolac was given. 5 mm of the drugs required every 15 days the areas underwent a gingival wash with an insulin syringe, which lasted for 3 months.

Detailed Description

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In this study, 40 patients with a history of Mild- Periodontitis who were diagnosed with clinical and radiographic findings showed that all of the periodontal parameters before the treatment, during the treatment period Then, scaling \& Root planing and oral hygiene instructions were given to the patients, and after 2 weeks, the patients who received the study were randomly divided into two groups (Balanced Block Randomization) with four blocks according to the visit time. To group A, oral chlorohexidine (Ghol Darou-Tehran) and to B group, the drug Ketorolac (Exir-Boroujerd) was given. 5 mm of the drugs required every 15 days the areas underwent a gingival wash with an insulin syringe, which lasted for 3 months. Pl, BI, PD were evaluated in the study sessions. At the end of the clinical change, a multiple measure ANOVA test was used to compare the preceding and follow-up sessions in both groups, considering the intervention method as Between subject comparison And measured at the time of measurement as a Repeated Factor.

Conditions

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Chronic Periodontitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

split mouth
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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ketorolac 3%

ketorolac 3% topical subgingival irrigation was put into the periodontal pocket using an insulin syringe

Group Type ACTIVE_COMPARATOR

Ketorolac

Intervention Type DRUG

Ketorolac 3% topical subgingival irrigation was put into the periodontal pocket using an insulin syringe

chlorhexidine 2%

chlorhexidine 2% topical subgingival irrigation was put into the periodontal pocket using an insulin syringe

Group Type OTHER

Chlorhexidine 2%

Intervention Type DRUG

Chlorhexidine 2% topical subgingival irrigation was put into the periodontal pocket using an insulin syringe

Interventions

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Ketorolac

Ketorolac 3% topical subgingival irrigation was put into the periodontal pocket using an insulin syringe

Intervention Type DRUG

Chlorhexidine 2%

Chlorhexidine 2% topical subgingival irrigation was put into the periodontal pocket using an insulin syringe

Intervention Type DRUG

Other Intervention Names

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Group A Group B

Eligibility Criteria

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Inclusion Criteria

40 patients with periodontitis chronic and has a 2 molar symmetrically in the lower jaw pockets of the periodontal depth of at least 5 mm and CAL 1-2 mm in at least one of the surfaces of the teeth, were selected

Exclusion Criteria

1. systemic disease
2. pregnancy or breastfeeding
3. allergy drug used
4. smoking
5. medication 6. not willing to consent to participate in the study

7-Trismus 8-The type of disease periodontal (Aggressive) 9. History of periodontal treatment in the previous 6 months 10-orthodontic treatment
Minimum Eligible Age

30 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Amirhossein Farahmand

OTHER

Sponsor Role lead

Responsible Party

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Amirhossein Farahmand

assistant prof

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Amirhossein Farahmand

Tehran, , Iran

Site Status

Countries

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Iran

Other Identifiers

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2037

Identifier Type: -

Identifier Source: org_study_id

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