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临床试验/CTRI/2026/02/104196
CTRI/2026/02/104196尚未招募2 期

A Clinico Microbiological Evaluation of the Effect of Herbal Extract on Peri Implant Microbial Profile and Marginal Bone Levels A Randomized Clinical Trial

Dr Gowri S Gaddadh1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年5月1日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
30
试验地点
1

研究概览

简要总结

This study is designed to evaluate the adjunctive effect of a five percent herbal extract gel containing Cissus quadrangularis and Curcuma longa when applied to the implant cover screw during dental implant placement in the test group while control group receives conventional peri implant therapy. Investigations include collection of peri implant sulcus samples at baseline and on the seventh post operative day of microbial analysis and assessment of crestal bone levels using CBCT immediately after surgery and at three months. Through comparative analysis between the test and control groups the study seeks to determine whether the herbal get provides antimicrobial benefits and promotes improved crestal bone preservation during early healing. The findings may contribute to evidence based to advancements in peri implant therapy and support the potential role of herbal adjuncts in enhancing implant success and peri implant tissue health.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patient aged above 18 years and below 65 years.
  • Periodontally and systemically healthy.
  • Partially edentulous patient with both teeth adjacent to the implant area.
  • A healed edentulous area with adequate hard and soft tissue.
  • No history of implant failure in that area.

排除标准

  • Patients with any evidence of systemic diseases such as diabetes mellitus, peripheral vascular disease, blood clotting disorders, or collagen vascular disease.
  • Any person who after blood investigations, are found to be HBsAg positive or HIV positive.
  • Any contraindications for implant placement.
  • Need for simultaneous soft and hard tissue augmentation.
  • History of allergy to any medications/ materials 6) Uncooperative patient/ patient diagnosed with intellectual disability 7) Presence/ History of periodontal disease 8) Pregnancy and lactation.

研究者

发起方
Dr Gowri S Gaddadh
申办方类型
Other [Dr Reshma Karkera]
责任方
Principal Investigator
主要研究者

Dr Reshma Karkera

Rajiv Gandhi Institute of Health Sciences, Bangalore 560041

研究点 (1)

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