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临床试验/NCT05744726
NCT05744726招募中不适用

Comparison of A-PRF vs Bone Wax in Hemostasis, Pain Relief and Healing Following Exodontia: A Single-blind Randomised Control Trial

Altamash Institute of Dental Medicine2 个研究点 分布在 1 个国家目标入组 129 人开始时间: 2023年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
129
试验地点
2
主要终点
Extraction socket healing

研究概览

简要总结

The goal of this clinical trial is to compare the pain relief and healing effect of A-PRF and Bone-wax in patients having mandibular tooth-extractions. The main question[s] it aims to answer are:

In the perspective of improvement in pain and healing;

  • Does A-PRF performs better than control group?
  • Does Bone-wax performs better than control group?
  • Healing index and Pain scale score Comparison of A-PRF and Bone-wax; if one is better than the other? Participants will be asked to give resoponse to a post-operative symptom severiety (PoSSe) scale. An investigator will score the patient's extraction for hemostasis and on healing index [describe the main tasks participants will be asked to do, treatments they'll be given and use bullets if it is more than 2 items]. If there is a comparison group: Researchers will compare [insert groups] to see if [insert effects].

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • All patients who need extraction of mandibular posterior teeth
  • Overall, systemically healthy individuals (Established based on history, i.e., patients who do not take medicine for any systemic condition).
  • INR within normal range.

排除标准

  • Patients with a diagnosed systemic condition.
  • Patients who are immunocompromised.
  • Patients who are unwilling to participate or withdraw from the study.
  • Patients who fail to report on the seventh and twenty-first post-extraction day.
  • Patients with physical or mental impairments who need assistance in taking their medications.

结局指标

主要结局

Extraction socket healing

时间窗: 21 days

Patients receiving any of the intervention will be evaluated at 3rd, 7th and 21st day of dental extraction on Healing index by Landry et al.

Pain Relief on VAS

时间窗: 21 days

Patients receiving any of the intervention will be evaluated at just before, 3rd, 7th and 21st day of dental extraction on Visual Analogue Scale (VAS).

次要结局

  • Hemostasis(30 minutes)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rehan Ahmad

Demonstrator/Lecturer

Altamash Institute of Dental Medicine

研究点 (2)

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