Effect of Orthodontic Treatment on Periodontally Compromised Dentition- Randomised Control Trial

Postgraduate Institute of Dental Sciences Rohtak

Status: Unknown

Conditions: Periodontal Bone Loss

Treatments: Procedure: Periodontal and orthodontic treatment; Procedure: periodontal treatment

Study type: Interventional

Funder types: Other

Identifiers

NCT03914339

meenu ortho

Details and patient eligibility

About

The main aim of this prospective, randomized controlled clinical study is to:

• To evaluate and compare the effect of a combined orthodontic -periodontal treatment protocol versus periodontal treatment alone on osseous and non -osseous parameters in periodontally compromised patients.

Full description

All the patients of both the groups will receive a detailed periodontal evaluation and then therapeutic management of patients will be done as per their periodontal requirement. This will include oral hygiene instruction, scaling and root planning and re-evaluation after 2 weeks and periodontal surgical treatment if indicated will be re-evaluated 4-6 weeks. After an observation period of 2 months confirming patient cooperation and their ability to maintain good oral hygiene as well as stability of the periodontal results orthodontic treatment will be started in the test group whereas the control group will be kept on monthly recall for the first 3 months and then every 3 months as per the oral hygiene status requirement of the patient.periodontal charting will be done at every 3 months till finish of treatment and supra gingival scaling will be provided as per requirement in both the groups.Changes in periodontal status in terms of clinical and radiographic parameters will be compared between the groups. cone beam Computed tomography will be taken at the baseline T0 and study end point T2 for assessment of changes in the bone level around maxillary and mandibular teeth

Enrollment: 36 estimated patients

Sex: All

Ages: 20 to 40 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

.• Patient age criteria 20-40 years.

• Periodontally Compromised dentition with moderate to severe periodontitis ≥2 teeth with pocket depth (PD) ≥5 mm and loss of clinical attachment level (CAL) ≥ 4mm. and radiographic bone loss
• Good general health status.
• Malocclusion that needs orthodontic treatment

Exclusion Criteria:

• Systemic illness known to affect the periodontium or outcome of periodontal and orthodontic therapy.
• Patient taking medications such as corticosteroids or calcium channel blockers, which are known to interfere periodontal wound healing or patient on long term NSAID therapy.
• Pregnant or lactating women.
• Smokers(≥5 cigarettes∕ day).
• Noncompliance to oral hygiene measures after Phase I therapy.
• Presence of trauma from occlusion (TFO).
• Patients with aggressive periodontitis

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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36 participants in 2 patient groups

Test group

Experimental group

Description:

Eighteen periodontally compromised patients who will be given both orthodontic and periodontal treatment .

Treatment:

Procedure: Periodontal and orthodontic treatment

control group

Active Comparator group

Description:

Eighteen periodontally compromised patients will receive periodontal treatment alone .

Treatment:

Procedure: periodontal treatment