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Clinical Trials/DRKS00004648
DRKS00004648Recruiting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 enrollmentStarted: February 25, 2013Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Recruiting
Sponsor
Enrollment
100

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomized controlled study
Masking
Open (masking not used)

Eligibility Criteria

Ages
18 Years to one (—)
Sex
All

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

Investigators

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

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