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Efficacy of warm humidified insufflation for reducing post-operative ileus.

Not Applicable
Withdrawn
Conditions
Presumed advanced ovarian malignancy
Presumed advanced tubal malignancy
Presumed advanced peritoneal malignancy
Cancer - Ovarian and primary peritoneal
Registration Number
ACTRN12618001419257
Lead Sponsor
Fisher and Paykel Healthcare
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Withdrawn
Sex
Female
Target Recruitment
226
Inclusion Criteria

Age 18 or older
Consented for Open Debulking surgery for presumed advanced ovarian, tubal or peritoneal malignancy.
Primary, Interval (after initial chemotherapy), or recurrent setting
Able to give informed consent and understand risks and benefits of the study

Exclusion Criteria

Active inflammatory bowel disease
Moderate to severe renal impairment (eGFR<50mL/min/1.73m2)
Severe hepatic impairment (Child-Pugh C)
Pregnancy
Pre-existing gut motility disorder including endocrine, metabolic or neurological cause
Pre-operative malnutrition requiring parenteral nutrition
Inability to give consent or participate in post-operative assessments due to dementia, cognitive impairment, language difficulties, delirium

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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