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临床试验/NCT06590870
NCT06590870已完成3 期

Intranasal Fentanyl for Procedural Analgesia in Preterm Infants Undergoing Peripherally Inserted Central Catheter Placement (INFENT PICC): a Feasibility Randomized Controlled Trial

Mount Sinai Hospital, Canada1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2024年8月9日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
8
试验地点
1
主要终点
Recruitment rate

研究概览

简要总结

The purpose of this feasibility clinical trial is to explore the role of intranasal fentanyl for pain associated with PICC placement in preterm infants. The primary goals are identifying whether enough infants join the study and complete the study procedures.

详细描述

Infants admitted to the neonatal intensive care unit (NICU) are subjected to multiple painful procedures as part of clinical care. It is established that early and repeated exposure to pain is associated with negative consequences. However, pain management strategies continue to be underutilized in NICUs worldwide.

Placement of a PICC is a clinically essential painful procedure in infants requiring prolonged intravenous access. The procedure can cause moderate to severe pain. To date, the optimal medication for procedural analgesia during PICC placement is not known.

Intranasal fentanyl has emerged as an option for pain management in infants admitted to the NICU. In preparation for a future definitive clinical trial, this is a feasibility clinical trial exploring the role of intranasal fentanyl for procedural analgesia in preterm infants undergoing PICC placement.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
0 Years 至 1 Year(Child)
性别
All
接受健康志愿者

入选标准

  • Infants with a gestational age at birth < 32 weeks or birth weight < 1.5 kg
  • Infants considered medically appropriate for the study by the most responsible physician

排除标准

  • Infants with choanal atresia, nasal mucosal erosion, or epistaxis
  • Infants with facial anomalies
  • Infants diagnosed with genetic conditions known to affect neurological development or severe (grade ≥ III) intraventricular hemorrhage
  • Infants receiving continuous intravenous infusions or scheduled enteral doses of opioids or sedatives within 12 hours of PICC placement
  • Infants with cardiopulmonary instability managed with inotropes, vasopressors, phosphodiesterase enzyme inhibitors, or neuromuscular blocking agents at the time of PICC placement
  • Infants prescribed strong CYP3A4 inhibitors (clarithromycin, itraconazole, ketoconazole, posaconazole, ritonavir, voriconazole) at the time of PICC placement
  • Infants diagnosed with bronchopulmonary dysplasia (need for supplemental oxygen or need for ventilatory support at 36 weeks corrected gestational age)
  • Infants with a previous documented adverse reaction to any formulation of fentanyl
  • Each eligible infant will be enrolled for one PICC placement only during the study period

研究组 & 干预措施

Intranasal fentanyl plus standard of care

Experimental

One dose of fentanyl 1.5 µg/kg via a mucosal atomization device 10 minutes before the PICC placement.

Standard of care includes sucrose 24% oral solution with or without non-nutritive sucking.

干预措施: Fentanyl (Drug)

Intranasal normal saline plus standard of care

Placebo Comparator

One dose of normal saline (volume equivalent to fentanyl 1.5 µg/kg) via a mucosal atomization device 10 minutes before the PICC placement.

Standard of care includes sucrose 24% oral solution with or without non-nutritive sucking.

干预措施: Normal saline (Drug)

结局指标

主要结局

Recruitment rate

时间窗: 6 month study period

Number of infants assessed for eligibility, number of infants approached for consent, number of enrolled infants, and number of participants completing study procedures

Completeness of data collection for pain score assessment

时间窗: At the needle insertion phase of the PICC placement

Premature infant pain profile-revised (PIPP-R) scores using video recordings. PIPP-R scores range from 0-21 and are interpreted as no pain (score of 0), mild pain (score 1-6), moderate pain (score 7-12), and severe pain (score 13-21).

次要结局

  • Number of adverse events(Up to 6 hours after intranasal intervention administration)
  • Acceptability and adoption of intranasal medications(Immediately after the PICC placement)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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