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临床试验/RBR-9xfmcc7
RBR-9xfmcc7招募中不适用

Effectiveness of using an Adhesive Dispenser in neonates admitted to an intensive care unit: a randomized clinical trial

Universidade Federal do Paraná - UFPR0 个研究点目标入组 728 人开始时间: 2026年6月8日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
728

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
0 至 29D(—)

入选标准

  • Neonates (up to 29 days of life, and considering corrected age for premature infants) of both sexes using endotracheal tube (ETT) fixation adhesive;Neonates of both sexes using polyurethane adhesive dressing on peripherally inserted central venous catheter (PICC)

排除标准

  • Neonates presenting previous skin alteration at the adhesive fixation site (ex: injury, erythema, urticaria, hyperpigmentation, hemangiomas, etc.); presenting any type of reaction to the dressing removal product;teing under phototherapy; presenting a confirmed diagnosis or suspicion of congenital epithelial syndromes; other orotracheal tube fixations different from those described in the protocol;anatomical alterations in the lip and chin region (e.g., cleft lip); presenting fluid or extravasation of infusion content at the insertion site of the peripherally inserted central venous catheter at the time of the intervention; legal guardian under 18 years of age or changing or removing the endotracheal tube fixation or PICC dressing in an emergency (non-elective) situation, for example: accidental extubation, accidental traction of the devices, clinical complications

研究者

发起方
Universidade Federal do Paraná - UFPR

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