Skip to main content
Clinical Trials/DRKS00004648
DRKS00004648
Recruiting
未知

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

Chirurgische Klinik IKlinik für Allgemein-, Viszeral- und Gefäßchirurgie und KoloproktologieJohanniter Krankenhaus Rheinhausen0 sites100 target enrollmentFebruary 25, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
postoperative analgesiapostoperative intestinal motility
Sponsor
Chirurgische Klinik IKlinik für Allgemein-, Viszeral- und Gefäßchirurgie und KoloproktologieJohanniter Krankenhaus Rheinhausen
Enrollment
100
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 25, 2013
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Chirurgische Klinik IKlinik für Allgemein-, Viszeral- und Gefäßchirurgie und KoloproktologieJohanniter Krankenhaus Rheinhausen

Eligibility 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

  • 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

Outcomes

Primary Outcomes

Not specified

Similar Trials