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临床试验/CTRI/2024/08/073071
CTRI/2024/08/073071尚未招募不适用

Comparative Assessment of Implant Placement by using Conventional Versus Flapless Technique: A Prospective Clinical Study

Dr Harvansh Singh Judge Institute of Dental Sciences And Hospital1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2024年9月9日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
32
试验地点
1
主要终点
1. duration of surgery

研究概览

简要总结

this is a randomized control clinical prospective study comparing the outcomes of conventional flap and flapless implant techniques in 32 patients over the course of 18 months. patients fulfilling inclusion criteria will be recruited and informed consent will be taken. following randomization, surgical procedure will be performed according to established protocol. preoperative assessments including clinical photographs and CBCT scans will be done to evaluate the implant site. surgical interventions will be meticulously executed with postoperative evaluation focusing on parameters such as surgical time, pain, swelling and marginal bone loss assessed using IOPAR and CBCT at designated intervals. post operative care instructions will be provided to ensure patients well-being and facilitate optimal healing.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
None

入排标准

年龄范围
25.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • 1.Age 25-55 years.
  • 2.Patients with edentulous spaces indicated for implant placement.
  • 3.Patients who are willing to comply with the treatment regimen.
  • 4.Patients with history of extraction not less than 6 months.
  • 5.Patients with health status ASA I & ASA II.
  • 6.Patients with adequate width of attached gingiva.

排除标准

  • 1.Pregnant females.
  • 2.Lactating mothers.
  • 3.Patients with uncontrolled systemic diseases contraindicating any type of surgery.
  • 4.Patients who are not willing to participate in the study or come for follow-up.
  • 5.Patients with any contraindications for implant placement.
  • 6.Patients undergoing radiation therapy or history of radiation therapy in head and neck region.
  • 7.Patients who are smokers and alcoholics.

结局指标

主要结局

1. duration of surgery

时间窗: 1. intraoperatively | 2. at night of surgery, day 1 to 7 | 3. at day 1, 3 and 7

2. pain

时间窗: 1. intraoperatively | 2. at night of surgery, day 1 to 7 | 3. at day 1, 3 and 7

3. swelling

时间窗: 1. intraoperatively | 2. at night of surgery, day 1 to 7 | 3. at day 1, 3 and 7

次要结局

  • marginal bone loss(at 1 month, 2 months and 3 months)

研究者

发起方
Dr Harvansh Singh Judge Institute of Dental Sciences And Hospital
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

PRATIBHA

Dr Harvansh Singh Judge Institute of Dental Sciences and Hospital, sector 25, Chandigarh

研究点 (1)

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