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临床试验/NCT01413789
NCT01413789已完成不适用

Measurement and Comparison of the Occlusive and Hydrating Capacity of Three Silicone Gels: BAP Scar Gel, Dermatix, Kelocote and One Gel- Cream: Alhydran

University Hospital, Ghent1 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2011年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
55
试验地点
1
主要终点
The occlusive and hydrating capacity of the products.

研究概览

简要总结

Study hypothesis: Is Alhydran gel-cream as efficient as silicone gel for skin occlusion and hydration?

For this study 16 volunteers and ten patients with healed full thickness burns will be included.

After a short period of acclimatization four test areas will be determined. For healthy volunteers the standard zones are located on the inner forearm, two on each forearm.

For patients with healed burns the 4 test zones are located on either the healed donor site or the healed skin grafted area.

In each test zone baseline measurements will be taken before application of the products.After application of the three silicone gels and the hydrating gel cream the trans epidermal water loss (TEWL) and the moisture content of the stratum corneum will be measured by using the TEWAmeter®TM300 and the Corneometer® CM825 (Courage & Khazaka).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • healthy volunteers or patients with healed full thickness burns and donor sites
  • not pregnant
  • age>18 years
  • male or female
  • written authorisation of the patient or volunteer is required.

排除标准

  • 未提供

研究组 & 干预措施

Patients and healthy volunteers

Experimental

Patients with healed full thickness burns and healthy volunteers will be included in the study

干预措施: Dermatix (Drug)

Patients and healthy volunteers

Experimental

Patients with healed full thickness burns and healthy volunteers will be included in the study

干预措施: Kelocote (Drug)

Patients and healthy volunteers

Experimental

Patients with healed full thickness burns and healthy volunteers will be included in the study

干预措施: BAP scar gel (Drug)

Patients and healthy volunteers

Experimental

Patients with healed full thickness burns and healthy volunteers will be included in the study

干预措施: Alhydran (Drug)

Patients and healthy volunteers

Experimental

Patients with healed full thickness burns and healthy volunteers will be included in the study

干预措施: Bap Scar Care T (Drug)

Patients and healthy volunteers

Experimental

Patients with healed full thickness burns and healthy volunteers will be included in the study

干预措施: Bap Scar Care S (Drug)

Patients and healthy volunteers

Experimental

Patients with healed full thickness burns and healthy volunteers will be included in the study

干预措施: Mepiform (Drug)

Patients and healthy volunteers

Experimental

Patients with healed full thickness burns and healthy volunteers will be included in the study

干预措施: Scar Ban Elastic (Drug)

结局指标

主要结局

The occlusive and hydrating capacity of the products.

时间窗: 1 hour after application

Measurements will be done by using the TEWAmeter® for measurement of the Trans Epidermal Waterloss and the Corneometer® 825CM for measurement of the moisture content of the stratum corneum (Courage \& Khazaka). For this study no risk factors are determined.

次要结局

  • The occlusive and hydrating capacity of the products.(3 hours after application)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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