Establishment of a measuring method for gastrointestinal tissue oxygenation to predict postoperative complications (Oxygen Saturation of Colon And Rectum)

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00021398

Enrollment

Registered

2020-05-29

Start date

2020-04-20

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

C20 C18

Interventions

Group 1: The perfusion of the intestinal wall is measured using O2C® (LEA medical technology, Giessen) in colonoscopies and resecting intestinal/rectal interventions with primary anastomosis.

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients in whom colonoscopy or abdominal surgery with partial bowel removal is required

Exclusion criteria

Exclusion criteria: Minority, pregnancy, inability to consent, rejection of the patient or lack of information.

Design outcomes

Primary

Measure	Time frame
- Difference in perfusion parameters at the excision margins in patients with and without anastomosis insufficiency measured with O2C® (LEA-Medizintechnik, Giessen)	—

Secondary

Measure	Time frame
- Parameter of perfusion ca. 10 cm ab ano in healthy patients - difference of perfusion after resection of the A. rectalis sup. - Calcium-Score in Aorta Abdominalis, Ae. iliacalis communis and internae	—

Countries

Germany

Contacts

Public ContactJulius Pochhammer

Klinik für Allgemeine, Viszeral-, Thorax-, Transplantations- und Kinderchirurgie UKSH Campus Kiel

julius.pochhammer@uksh.de+49 431 500 20413

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026