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临床试验/NCT03677297
NCT03677297已完成4 期

Comparative Evaluation of Treatment Of Infrabony Defects With and Without 1.2% Rosuvastatin Gel: In-Vivo Study

Dr. D. Y. Patil Dental College & Hospital1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2016年1月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
10
试验地点
1
主要终点
Bone fill

研究概览

简要总结

Study aims to evaluate clinical and radiographic effectiveness of 1.2% Rosuvastatin gel in the treatment of Infrabony defects in chronic periodontitis patients.

详细描述

Source from where the patients will be selected:

10 patients with chronic periodontitis having two or more infrabony defects will be selected from the Outpatient section of Dept. of Periodontology, Dr. D. Y. Patil Dental College and Hospital, Pimpri, Pune - 18.

A detailed clinical examination, case history and written consent will be obtained from all the participants.

Before surgery, each patient will be given careful instructions regarding proper oral hygiene measures. A full-mouth phase I therapy will be performed. A periodontal re-evaluation will be performed after 4 to 6 weeks of phase 1 therapy to confirm the desired sites for the study. The selected sites will be divided randomly by using a Sequentially numbered, opaque, sealed envelopes (SNOSE) randomization into control and test sites. The control site will be treated with Access Flap Surgery (AFS), whereas test sites will be treated with AFS and 1.2% Rosuvastatin gel. Suitable antibiotics and analgesics will be prescribed along with Chlorhexidine digluconate rinses (0.2%) twice daily for 14 days. Patients will be examined at 4 weeks, 3 and 6 month after surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
30 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age group between 30-50 years
  • Probing pocket depth ≥ 5mm following initial therapy.
  • Suitable interproximal angular infrabony defects of ≥3mm.
  • Involved teeth should be vital and asymptomatic.
  • Systemically healthy patients.
  • Patients who demonstrate acceptable oral hygiene prior to access flap surgery.
  • Patients agreed to sign informed consent and willing to return for the follow up visits.

排除标准

  • Systemic statin therapy
  • Known or suspected allergy to the statin group
  • Allergy to sulfur containing drugs
  • History of aggressive periodontitis.
  • Presence of gingival recession at the surgical site.
  • Mobility of study teeth ≥ grade I.
  • Use of tobacco in any form.
  • Pregnant and lactating women.
  • patients who have received any anti-inflammatory drugs and antibiotics in the previous six months.
  • H/O osteoporosis.

研究组 & 干预措施

ROSUVASTATIN

Experimental

1.2% Rosuvastatin Gel. Insertion in infrabony defects once

干预措施: Rosuvastatin (Drug)

placebo

Placebo Comparator

No intervention used on control site

干预措施: Rosuvastatin (Drug)

结局指标

主要结局

Bone fill

时间窗: 6 months

Radiographic parameter measuring distance from cemento-enamel junction to the base of the defect. Difference in the measurement at the end of 6 months shows the amount of bone fill

次要结局

  • Probing depth(6 months)
  • relative attachment level(6 months)
  • plaque index(6 months)
  • bleeding index(6 months)

研究者

发起方
Dr. D. Y. Patil Dental College & Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

DR. SUKHADA DEO

Principal investigator

Dr. D. Y. Patil Dental College & Hospital

研究点 (1)

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