PACTR201803003085193Other未知
The impact of healing protocol and attachment type for single-implant retained mandibular complete dentures: protocol for a randomized controlled trial.
prosthodontic department0 个研究点目标入组 80 人开始时间: 2018年2月12日最近更新:
试验速览
- 阶段
- 未知
- 状态
- Other
- 发起方
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 50 Year(s) 至 69 Year(s)（—）
- 性别
- All
入选标准
- •Completely edentulous male or female patients between the ages of 50 to 69.
- •-No contraindications for implantation.
- •-Each patient has to perform both a random blood sugar and Glycosylated Hemoglobin analysis. Patients with a Glycosylated hemoglobin test HbA1c up to 8% and a normal blood sugar level (79 to 110) or controlled diabetes (90-130 fasting according to American Association of Diabetes) will be included.
- •-Sufficient bone width (¿ 5 mm) in the anterior region to place an implant. It could be either normally present or achieved by bone plateauing. This will be confirmed by cone beam computed tomographic (CBCT) scans.
- •-Residual bone height is 11-20 and 13 mm as the lowest vertical height of the mandible and the lowest vertical bone height in the midline of the mandible, respectively (Class II or III according to McGarry et al. 1999.
- •-Patients seeking to install a single median implant in the mandible and for whom new dentures will be constructed.
- •-Patients, who are dissatisfied with the retention and stability of their technically satisfactory mandibular dentures.
- •-Patients, who already have existing maxillary and mandibular complete dentures, and after examination of the mandibular dentures, it is found that there are technical problems with regard to denture design and/or occlusion; then new maxillary and mandibular dentures will be fabricated.
- •-All patients should have adapted to their dentures for at least six weeks before being included in the trial.
- •-Provide a written consent to participate in the trial, and this will be done before the scheduled date for implant installation.
排除标准
- •-Patients with a systemic or local contra-indication for implant placement.
- •-Satisfied patients with the retention of their mandibular denture as well as unsatisfied patients with their maxillary denture.
- •-Patient with a mandibular denture height less than 6 mm between the base of the denture and the incisal edge of the central incisors (this was measured by a caliper).
- •-Patients who are classified as Class I, or IV according to McGarry et al. 1999.
- •-Incompliant and not cooperative patients.
- •-Patients with an implant stability less than 60 ISQ (this is not an exclusion criteria in this phase, this would be considered during implant installation).
研究者
相似试验
招募中
不适用
Rehabilitation of patients after meniscus surgeryMENISCUS INJURYC26.558.781RBR-95c4rdniversidade Federal de Santa Catarina
招募中
不适用
Effect of Customized Healing Abutment on alveolar ridge contourIRCT20220702055345N1Islamic Azad University26
招募中
Unknown
Investigating the effect of customized healing piece on alveolar ridge contourAlveolar ridge width.Atrophy of edentulous alveolar ridgeK08.2IRCT20180714040460N10Islamic Azad University26
已完成
不适用
Effect of Enhanced Recovery Protocol versus Conventional Protocol on Patients Outcome in Colorectal SurgeriesDigestive SystemSurgeryCancerPACTR201901464065582Department of Anesthesia and Surgical Intensive Care Faculty of Medicine Alexandria University30
尚未招募
不适用
a study to compare early removal of tubes and early feeding against standard treatment which is delayed feeding and delayed removal of tubes to see for early recoveryCTRI/2019/06/019533ALL INDIA INSTITUTE OF MEDICAL SCIENCES NEW DELHI