C20 D12.8
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age = 18 years, planned elective rectal resection, placement of a postoperative drain near the anastomosis or surgical site (standardized procedure), written informed consent
Exclusion criteria
Exclusion criteria: Emergency surgeries, pre-existing chronic inflammatory bowel disease (e.g. Crohn's disease, ulcerative colitis), systemic, chronic inflammatory or autoimmune diseases (e.g. rheumatoid arthritis, active infectious diseases)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Course of calprotectin levels in serum and drainage fluid (on days 1, 3 and 5 postoperatively) in patients after rectal resection. | — |
Secondary
| Measure | Time frame |
|---|---|
| Primary study objective: Monitoring the course of calprotectin levels in serum and drainage fluid (preoperatively, on days 1, 3, and 5 postoperatively) in patients after rectal resection. Secondary study objectives: Comparison of the dynamics of calprotectin with conventional inflammatory markers (CRP, PCT, leukocytes) in the blood. Investigation of drainage fluid parameters (cell count, pH, lactate) and their relationship to calprotectin. Does the type of resection (e.g., with/without neoplasia) or surgical approach (open vs. minimally invasive) influence calprotectin levels? Tertiary study objective: Should complications (such as anastomotic leakage) occur, can a trend in calprotectin (increase in laboratory parameters) be demonstrated? | — |
Countries
Germany
Contacts
Krankenhaus Agatharied