DRKS00033789已完成Unknown
A randomized, controlled trial comparing the use of the Endoflator 50® (KARL STORZ SE & CO. KG) to not preheated optic
niversitätsklinikum des Saarlandes, Klinik für Frauenheilkunde, Geburtshilfe und Reproduktionsmedizin0 个研究点目标入组 73 人开始时间: 2024年3月18日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 73
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
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- Female
入选标准
- •informed consent
- •Age over 18 years
- •Indication for laparoscopy
- •ASA Risk Classification I-II
排除标准
- •No informed consent
- •Pregnancy. This is validated preoperatively via a pregnancy test (urine), not older than 24 hours
- •Allergies to the anti-fog agents used
- •Phemoperitoneum or severe ascites
- •ASA = III
- •Duration of operation less than 30 min
研究者
相似试验
已完成
不适用
Comparison of FemSoft® urethral insert and vaginal tampons for stress urinary incontinenceFemale stress urinary incontinenceUrological and Genital DiseasesStress incontinenceISRCTN97985616Rochester Medical Ltd (UK)90
已完成
不适用
A randomised controlled trial comparing the use of sirolimus based biphasic immunosuppression with myfortic to allow early CalciNeurin Inhibitor (CNI) withdrawal in renal transplantatioRenal transplantationInjury, Occupational Diseases, PoisoningISRCTN76390219niversity Hospitals of Leicester NHS Trust (UK)42
Unknown
2 期
Are drains really necessary for patients undergoing parotid surgery?CTRI/2019/07/020209FLUID RESEARCH GRANT CMC VELLORE45
尚未招募
2 期
A randomised controlled trial evaluating the use of Motivational Interviewing compared to usual care to increase physical activity in people living in the community after a hip fracturehip fracture rehabilitation - increasing activityhip fracture rehabilitation - quality of lifehip fracture rehabilitation - mental healthMusculoskeletal - Other muscular and skeletal disordersACTRN12613000680763Dr Paul O'Halloran from La Trobe University24
进行中（未招募）
1 期
Prospective, randomised trial comparing the use of Tisseel versus no fibrin sealant in preventing postoperative fluid complications following liver resection - Tisseel 1EUCTR2006-002332-17-GBThe Leeds Teaching Hospitals NHS Trust242