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Clinical Trials/ISRCTN87898051
ISRCTN87898051
Completed
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 sites68 target enrollmentJune 26, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
aparoscopic abdominal surgery for a benign gynaecological condition
Sponsor
niversity Malaya Medical Centre Obstetrics & Gynaecology Department
Enrollment
68
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

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

Registry
who.int
Start Date
June 26, 2019
End Date
December 31, 2019
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
niversity Malaya Medical Centre Obstetrics & Gynaecology Department

Eligibility Criteria

Inclusion Criteria

  • 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)

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Not specified

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