ACTRN12621000396820已完成未知
A randomised controlled trial comparing the efficacy of conventional absorbable sutures and knotless absorbable sutures using a split-mouth design.
igel Tan0 个研究点目标入组 70 人开始时间: 2021年4月9日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 70
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 44 Years(—)
- 性别
- All
入选标准
- •1.Patients referred for third molar removal from a primary care provider
- •2.Patients who volunteer participation
- •3.Patients may be either male or female
- •4.The patient has been screened by the primary investigator or supervising specialist for suitability to participate in the study
- •5.Are aged between 18 and 44 years
- •6.Are able to understand verbal and written instructions.
- •7.Present with bilateral similarly impacted mandibular third molars as determined using Winter’s (1926) classification system , requiring surgical removal
- •8.Are able to tolerate outpatient oral surgery under local anaesthetic and intravenous sedation
- •9.ASA l or ll
- •10.The patient has provided informed consent regarding:
- •a.Participation in the study
- •i.The use of knotless sutures in the closure of the surgical wound
- •b.Surgical removal of third molars under local anaesthetic and intravenous sedation
排除标准
- •1.American society of anaesthesiologists (ASA) physical classification III or IV
- •2.Polypharmacy (greater than or equal to 5) medications
- •4.Patients contraindicated to undergo surgical third molar removal
- •5.Patients contraindicated to treatment under monoagent midazolam IV sedation
- •6.Opioid and illict drug addiction
- •7.Patients that have allergies or contraindications to the procedural usage of:
- •a.midazolam
- •b.dexamethasone
- •c.parecoxib
- •d.paracetamol
- •e.ibuprofen
- •f.co-amoxiclav
- •g.cefazolin
- •h.clindamycin
- •i.chlorhexidine
- •8.The presence of symptomatic pericoronitis.
- •9.The presence of other pathology in the oral cavity.
- •10.Patients with poor oral hygiene (plaque >1/3 of tooth surface).
- •11.Pregnant or lactating women.
- •12.Male patients who do not agree to facial hair removal.
- •13.Patients who are unable to give informed consent.
- •14.Patients who decline participation.
- •15.Patients who are unable to attend the required follow-up appointments.
- •16.Patients who are unable to comprehend directions and instructions.
- •17.Patients unwilling to trim facial hair for the purposes for the measurement of facial swelling
研究者
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