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临床试验/NCT07084194
NCT07084194尚未招募不适用

Impact of Integrating Two Nano Based Irrigants With Two Activation Techniques in Treatment of Teeth With Acute Pulpitis on Postoperative Pain and Flare up Incidence: A Randomized Clinical Study

Minia University0 个研究点目标入组 64 人开始时间: 2025年9月10日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
64
主要终点
postoperative pain intensity Postoperative pain is to be assessed using visual analog scale (VAS), A scale from (0 to 10) where "0" means no pain and "10 means a severe pain that has never faced before.

研究概览

简要总结

This study aimed to evaluate and compare impact of integrating passive ultrasonic activation and laser activation with nano-chitosan and aloe vera in terms of postoperative pain and flare-up incidence in a randomized clinical trial.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Age 18-60 (adults only)
  • multiple-rooted with multiple root canal.
  • Permanent teeth with mature apex and complete root formation.
  • Without root caries.
  • Tooth must be restorable.
  • Without anatomical abnormalities such as fusion.
  • Healthy patient category I according to ASA.
  • Vital tooth, with acute irreversible pulpitis and without peri-apical periodontitis.
  • No periapical radiolucency.
  • Consent Patients for who consent to participate and attend follow-up appointments.

排除标准

  • single root canals or double root.
  • Root canal calcifications.
  • Root resorption or fracture.
  • Previously root canal treated teeth.
  • immunocompromised patients.
  • Pregnant females
  • Patients with systemic diseases as diabetic or hypertension patients.
  • Patients with facial swelling.
  • patients who use analgesics or antibiotics within 48-72 hours.
  • Allergy to any materials used (e.g., irrigants or anesthetics).
  • psychiatric illness
  • Teeth that are not indicated for endodontic treatment: bad oral hygiene, mobile teeth, or recessed teeth.
  • Previously endodontically treated teeth.
  • Teeth with sinus tract.

结局指标

主要结局

postoperative pain intensity Postoperative pain is to be assessed using visual analog scale (VAS), A scale from (0 to 10) where "0" means no pain and "10 means a severe pain that has never faced before.

时间窗: [Time Frame: 6, 12, 24, 48, 72 hours and 7 days after the first visit to collect the postoperative pain data.]

Patients will be contacted by phone at 6, 12, 24, 48, 72 hours and 7 days after the first visit to collect the postoperative pain data.

次要结局

  • Flare-Up Incidence Flare-up is assessed through asking the patient to notify the investigator if any sudden severe pain or swelling takes place.([Time Frame: Within 7 days post-treatment))

研究者

发起方
Minia University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Rabee Ibrahaim Ismail Alhabibi

Rabee Alhabibi

Minia University

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