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临床试验/CTRI/2024/11/077058
CTRI/2024/11/077058尚未招募4 期

Evaluating the efficacy of application of i-prf on implant stability and marginal bone levels: A randomized clinical study

Jyothi Prasanna Paritala1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年11月28日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Implant stability measurement,

研究概览

简要总结

A randomized single blinded clinical study will be conducted. A total number of 30 implants will be  placed in edentulous spaces in both maxilla and mandible in systemically healthy patients. Patients will be selected based on inclusion criteria. Informed consent will be taken from the patients.Patients were examined clinically, and the residual bone will be evaluated using a CBCT. Blood examinations will be obtained to make sure the individuals were ideal candidates. Each 15 implants**(NORIS,Int.HexTi.Tufted implant)** will be randomly allocated to Test  (with I-PRF) and Control (without I-PRF) groups.Implant stability will be measured in 2 groups immediately after implant placement (baseline),10 days,1 month, 3 months and 6 months and marginal bone levels will be measured at 3 and 6 months.All the parameters will be recorded by other operator to avoid Bias.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • i)Systemically healthy patients(ASA I,II).
  • ii)Patients with Stable occlusion.
  • iii)Adequate bone height and width at the surgical site.
  • iv)Adequate mesiodistal and interocclusal spaces in the edentulous area.

排除标准

  • â—¦Presence of active periodontal disease.
  • â—¦Pregnancy or Lactation women.
  • i)Patients with any systemic disease and medications that will interfere with treatment outcome.
  • ii)History of radiotherapy or chemotherapy.
  • iii)Primary stability less than 25 Ncm during fixture placement.

结局指标

主要结局

Implant stability measurement,

时间窗: Baseline,10 days,1 month, 3 months and 6 months

Radiographic evaluation

时间窗: Baseline,10 days,1 month, 3 months and 6 months

次要结局

  • Radiographic evaluation(3 months and 6 months)

研究者

发起方
Jyothi Prasanna Paritala
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Jyothi Prasanna Paritala

GSL Dental College and Hospital

研究点 (1)

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