CTRI/2023/09/058011尚未招募Unknown
Post marketing clinical follow up (PMCF) evaluation of safety and performance of Accuflow VE- Syringe Pump. - NI
vTitan Corporation Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Subjects willing to participate in the study.
- •Subjects requiring intermittent or continuous infusion of fluid, medication or nutrients.
排除标准
- •Subjects not willing to participate in the study.
- •Subjects with a history of hypersensitivity to the medication being infused.
- •Subjects with a history of hypersensitivity to the syringe pump components.
- •Subjects having pain or swelling at infusion site.
研究者
相似试验
招募中
4 期
A study to evaluate the safety and tolerability of nasal dressing (VELNEZ) after a nasal surgery.CTRI/2024/06/068328Datt Mediproducts Pvt Ltd,
招募中
4 期
To study the effectiveness of surgical treatment in patients with knee joint paiCTRI/2023/12/060753Auxein Medical Pvt Ltd
招募中
Unknown
Elbow bone injuryCTRI/2024/01/061499Auxein Medical Pvt Ltd
招募中
4 期
ower leg bone fracture studyCTRI/2022/12/048209Kaulmed Pvt. Ltd.
已完成
不适用
Post-market clinical follow-up (PMCF) study to observe the course of symptoms of vulvovaginal dryness in patients receiving therapy with KadeFungin® BefeuchtungsgelN89.8Other specified noninflammatory disorders of vaginaDRKS00017248DR. KADE Pharmazeutische Fabrik GmbH100