From ACute To Chronic Postoperative Pain in Patients for Elective Cholecystectomy

NCT01553253 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2014-06-17

No results posted yet for this study

Summary

Chronic Pain is a wellknown complication after cholecystectomy. Intensity of the pain in the first week after the operation is a predictive factor for the development of chronic pain, but it is unknown whether the risk is more related to one of the different components of acute pain (ie somatic, visceral, referred). Furthermore the chronic pain has not been systematically described in terms of type of pain or sensory abnormalities etc. (allodynia, hyperalgesia etc.).

The purpose of the study is to examine whether intensity of components of acute pain is predictive for development of chronic pain after cholecystectomy and to characterize the chronic pain by quantitative sensory testing.

DNA-samples are collected to examine genetical factors, important for perception of pain, and the development of chronic pain.

Conditions

Sponsors & Collaborators

  • University of Southern Denmark

    collaborator OTHER
  • Region of Southern Denmark

    collaborator OTHER
  • Vejle Hospital

    collaborator OTHER
  • Manufacturer Mads Clausen Foundation

    collaborator OTHER
  • DASAIMS Forskningsinitiativ

    collaborator UNKNOWN
  • Fonden Else Poulsens Mindelegat

    collaborator UNKNOWN
  • Oberstinde Kirsten Jensa la Cours Foundation

    collaborator OTHER
  • Læge Frk. K. Rasmussens Mindelegat

    collaborator UNKNOWN
  • Odense University Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2012-06-30
Completion
2012-06-30

Countries

  • Denmark

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01553253 on ClinicalTrials.gov