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临床试验/NCT03029195
NCT03029195已完成不适用

Efficacy of Nasoalveolar Molding Therapy for Treatment of Unilateral Cleft Lip and Palate in Egyptian Infants

Alexandria University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Three dimensional (3D) change in the maxillary geometry.

研究概览

简要总结

The cleft lip and palate (CLP) is the commonest craniofacial anomaly worldwide. Nasoalveolar molding (NAM) therapy has emerged in the management of CLP as an early presurgical intervention to provide symmetry to severely deformed nasal cartilage, achieve projection to the flattened nasal tip, provide nonsurgical elevation for the columella, improve alignment of the alveolar ridge, reduce the cleft gap and it could significantly reduce the number of secondary surgeries. Despite that NAM therapy is becoming the treatment option for early cleft care, there is growing debate about its efficacy due to lack of quantitative assessment of these findings. To provide the highest levels of clinical evidence on NAM therapy, there has been international call for Randomized Controlled Clinical Trials.

Statement of the problem: lack of quantitative data about the efficacy of the NAM therapy for unilateral CLP.

Aim of the study: is to develop a standardized non-invasive quantitative assessment for two different techniques of the NAM therapy in Egyptian infants that involves 3D laser scanning/CAD analysis for maxillary geometry, and nasal anthropometric analysis.

Methods Trial design: Prospective randomized controlled clinical trial (RCT). Settings: The RCT will be performed through two phases; (Phase I: A controlled pre and post-RCT that will be designed for the quantitative evaluation of the NAM therapy on the maxillary geometry), and (Phase II: A post-test RCT will be designed for the quantitative evaluation of the NAM therapy on the nasal anthropometry and comparing the outcome with the nasal anthropometry that will be performed to age matched Egyptian norms).

Participants: 30 Egyptian infants with nonsyndromic UCLP will be randomly allocated to study groups (Group I, n=15) that will undergo NAM therapy before the primary surgical repair, and control group (n=15) that will undergo the primary surgical repair without NAM therapy. And 15 Egyptian infants will act as norm group.

Follow-up: (phase I- T0: before NAM, T1: after 1 month and T2: before surgery). (Phase II- T"0: 10 days after surgery, and T"1: 6 months after surgery).

详细描述

o Trial Design:

The present randomized controlled clinical trial (RCT) will be performed through two phases:

• RCT- (Phase I)

A controlled pre- and post-clinical trial will be designed for the quantitative evaluation of the NAM therapy on the maxillary geometry.

• RCT- (Phase II)

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 (Outcomes Assessor)

入排标准

年龄范围
1 Day 至 30 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Egyptian infants.
  • Infants should present with nonsyndromic complete UCLP ,
  • Infant age should be less than 90 days.
  • The infant's family agreed to undergo NAM therapy.

排除标准

  • Congenital malformations and soft tissue bands.

结局指标

主要结局

Three dimensional (3D) change in the maxillary geometry.

时间窗: (T0 baseline; pre-NAM therapy), (T2 during NAM therapy) and (T3 before surgery)

CAD analysis for the maxillary casts that will be obtained from the cleft infants in both study and control group.

次要结局

  • Change in the nasal anthropometry.(( T"0 = 1 days post-surgery) and (T"1= 6 months post-surgery).)

研究者

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

Mona Sabry Mostafa Saad

Lecturer of Prosthodontics

Alexandria University

研究点 (1)

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