ISRCTN87898051Completed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 enrollmentStarted: June 26, 2019Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 68
Study Overview
Brief Summary
2012 Results article in https://doi.org/10.1186/s12905-022-01696-z (added 19/07/2023)
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Sex
- Female
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
Investigators
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