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Postoperative analgesia and postoperative influences on intestinal motility of peridural anaesthesia versus continous preperitonal wound infusion of ropivacaine 0.2% following elective laparotomy - a prospective, randomized, controlled, non-blinded study

Postoperative analgesia and postoperative influences on intestinal motility of peridural anaesthesia versus continous preperitonal wound infusion of ropivacaine 0.2% following elective laparotomy - a prospective, randomized, controlled, non-blinded study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00004648
Enrollment
100
Registered
2013-02-25
Start date
2013-01-02
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

postoperative analgesia postoperative intestinal motility R52.9

Interventions

Group 1: Procedure 1: Peridural catheter (PDA) - preoperative placement of the PDA by the anaesthetists - postoperative continous application of ropivacaine 0.2% 6-8ml/h via perfusor - dolorimetry i

Sponsors

Chirurgische Klinik I Klinik für Allgemein-, Viszeral- und Gefäßchirurgie und Koloproktologie Johanniter Krankenhaus Rheinhausen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: - all elective operations concerning resections of the gastrointestinal tract of benign and malignant character (oesophagus, stomach, panreas, liver, small intestine, colon) - median laparotomies, transverse epigastric laparotomies - clean and clean-contaminated operations - minimum 18 years old patients - capability to understand and sign the objectives of the study, patient information and informed consent

Exclusion criteria

Exclusion criteria: exlusion criteria: - emergeny operations - chronic pain-disorder patients with a continuous analgesic medication - allergic disposition for amide anaesthetics - patient with chronic defecation diseases (ODS, long bowel syndrome) - pregnant and breast-feading women - underage patients - refusal by patient - disability to understand the patient information and sign the informed consent - infections in the puncture area respectively systemic infections

Design outcomes

Secondary

MeasureTime frame
Secondary outcome: period of hospitalisation, cost efficiency, rang of risks.—

Primary

MeasureTime frame
Primary outcome: dolorimetry pain postoperative and peristalsis postoperative. Dolorimetry postoperative pain and postoerative peristalsis in the evening of the operation day and postoperative day 1-3 in the morning, at noon and in the evening by the numeric scale and by auscultation.—

Countries

Germany

Contacts

Public ContactAnne Sabine Vetter

Chirurgische Klinik I Klinik für Allgemein-, Viszeral- und Gefäßchirurgie und Koloproktologie Johanniter Krankenhaus Rheinhausen

a.vetter@johanniter-rheinhausen.de02065-97-1201

Outcome results

None listed

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