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临床试验/ISRCTN87898051
ISRCTN87898051已完成未知

Post LaparoscopY Pain Reduction Project I (POLYPREP I): Single Strategy of Intraperitoneal Normal Saline Infusion (INSI); A Randomised Controlled Trial

niversity Malaya Medical Centre Obstetrics & Gynaecology Department0 个研究点目标入组 68 人开始时间: 2019年6月26日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
68

研究概览

简要总结

2012 Results article in https://doi.org/10.1186/s12905-022-01696-z (added 19/07/2023)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Women aged 18 years and above
  • 2. Scheduled for laparoscopic surgery for benign gynaecological condition
  • 3. American Society of Anaesthesiologist (ASA) classification I-II:
  • ASA I – normal healthy patient
  • ASA II – patient with mild systemic disease without substantive functional limitations (BMI < 40 kg/m2, well-controlled diabetes mellitus / mild hypertension, mild lung disease)

排除标准

  • 1. Conversion to laparotomy
  • 2. Allergy to non-steroidal anti-inflammatory drugs (NSAID) drugs or paracetamol
  • 3. Pre-operative emphysema / chronic obstructive pulmonary disease (COPD)
  • 4. Women who do not understand the questionnaire
  • 5. Pre-existing shoulder pain
  • 6. Intellectual disability

研究者

发起方
niversity Malaya Medical Centre Obstetrics & Gynaecology Department

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