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The effect of pneumoperiteum during laparoscopic surgery on the paediatric intestine

The effect of pneumoperiteum during laparoscopic surgery on the paediatric intestine - Pneumoperitoneum on paediatric intestine

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36223
Enrollment
32
Registered
2011-05-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

minimal invasive surgery pneumoperitoneum

Interventions

None listed

Sponsors

Medisch Universitair Ziekenhuis Maastricht
Lead Sponsor

Eligibility

Age
2 Years to 17 Years

Inclusion criteria

Inclusion criteria: Age

Exclusion criteria

Exclusion criteria: Diagnosis of necrotizing enterocolitis, because of prior elevated iFABP Emergency surgery Inflammatory bowel disease, or other bowel disorders, which can cause iFABP elevations.

Design outcomes

Primary

MeasureTime frame
Peroperative measurements of: • Urinary iFABP: as a measurement of the ischemia in the intestines (Detection limit 40pg/ml pg/ml). Urinary samples are taken each 10 minutes during the pneumoperitoneum, because of the half time of 11 minutes for iFABP. A control sample is taken before the start of the pneumoperitoneum and the last sample is taken 10 minutes after surgery. • Urinary Creatinin: to calculate iFABP/ creatinin ratio (cut off point 2.2 pg/nmol). In the same samples as iFABP • Intra-abdominal pressure and insufflation flow on monitor are registered in the same 10 minutes interval as the urine samples

Secondary

MeasureTime frame
Post-operative measurement of: • Urinary iFABP: Urinary samples by active urination of the patient, after the removal of the urinary catheter (the time is noted), until 24h after the surgery. • Urinary Creatinin: In the same samples as iFABP • Restoration of Gastro-intestinal function (per 6h in the first 24h; daily in the first week) (First defecation, first oral feeding, and full oral feeding) • Hospital stay in days

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)