跳至主要内容
临床试验/ACTRN12611000852954
ACTRN12611000852954已完成2 期

Randomised, double-blinded clinical trial comparing intranasal and intramuscular naloxone for reversal of suspected opioid overdose in clients of the Sydney Medically Supervised Injecting Centre

Sydney Medically Supervised Injecting Centre0 个研究点目标入组 200 人开始时间: 2011年8月10日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • All clients with symptoms/signs of an opioid overdose requiring Naloxone administration will be eligible for entry. This is based on existing and approved MSIC protocols and clinical criteria for overdose (reduced level of consciousness as measured by the Glasgow Coma Score, pinpoint pupils, respiratory depression and/or reduced oxygen saturations as measured by pulse oximetry).

排除标准

  • Less than 18 years of age
  • Pregnant or suspected of being pregnant

研究者

发起方
Sydney Medically Supervised Injecting Centre

相似试验

已完成
3 期
A double-blind, randomized clinical trial comparing S-1 in combination with DC vaccine loaded with WT1 peptides (TLP0-001) or placebo for the patients with advanced pancreatic cancer refractory to standard chemotherapy.pancreatic cancer
JPRN-UMIN000027179Wakayama Medical University185
招募中
不适用
TAP-studyElective mentally competent surgical patients for open inguinal hernia repair in daytime surgeryDe onderzoekspopulatie bestaat uit wilsbekwame proefpersonen ouder dan 18 jaar die zich op de preoperatieve screening van de polikliniek van de afdeling anesthesiologie in het Westfriesgasthuis presenteren voor een operatieve correctie van een liesbreuk volgens Lichtenstein en die voldoen aan de in en exclusie criteria zoals hieronder vermeld. De proefpersonen worden geïncludeerd na informed consent.
NL-OMON25473Westfries medical center Hoorn60
已完成
不适用
A randomised, double blind clinical trial comparison the effect of a ultrasound-guided transversus abdominis plane (TAP) block and wound infiltration on postoperative pain (48h) for open inguinal hernia repair in day-carepost-operative pain after inguinal hernia repair10041297
NL-OMON42102Westfries Gasthuis60
进行中(未招募)
1 期
A trial on comparison the effect of a TAP-blok and wound-infiltration on pain after inguinal hernia repair surgeryPostoperative pain after hernia inguinalis repair surgeryMedDRA version: 17.0Level: LLTClassification code 10036236Term: Postoperative pain reliefSystem Organ Class: 100000004865
EUCTR2014-002595-82-NLWestfriesgasthuis
进行中(未招募)
不适用
Double-blind, randomized, clinical trial to compare the efficacy and safety of diclofenc 3% gel vs. Solaraze 3% gel vs. vehicle for the treatment of patients with actinic keratosis.actinic keratosis
EUCTR2011-003317-41-DEDermapharm AG