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Clinical Trials/NCT02383342
NCT02383342Active, not recruitingNot Applicable

Development of Postoperative Pain; Clinical and Genetic Factors

Radboud University Medical Center1 site in 1 country10,000 target enrollmentStarted: May 12, 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
10,000
Locations
1
Primary Endpoint
Genetic risk factors for the development of acute pain using a visual analogue scale.

Study Overview

Brief Summary

Pain is the most frequent cause of suffering and disability in society. Despite considerable involvement of genetic factors in pain sensation and sensitivity, the individual genes involved remain largely unidentified.

In this project the investigators will follow patients undergoing elective major surgery for the development of acute and chronic pain. The investigators will search for clinical as well as genetic factors that can predict the development of pain. These can serve as biomarkers to predict acute and chronic pain development and progression in individual patients and help early individual treatment adaptation.

Detailed Description

Pain is the most frequent cause of suffering and disability in society. Chronic pain seriously impairs quality of life of millions of people worldwide. 10-50% of surgical patients report chronic pain after surgery; up to 10% report severe pain. Thus, chronic pain is a significant medical and financial burden to society.

Despite considerable involvement of genetic factors in pain sensation and sensitivity, individual genes involved remain largely unidentified. Knowledge of genetic factors, their phenotypic expression in pain processing, and their link to neuronal correlates can improve understanding of pain aetiology and processes involved in pain perception and chronification. Also, they can serve as biomarkers to predict chronic pain development and progression in patients and help early individual treatment adaptation.

In this study the investigators will establish a prospective database and biobank of patients undergoing elective major surgery. Using data from the database and biobank, the investigators will identify genetic factors contributing to development of acute and chronic pain after surgery.

Over a period of 10 years the investigators will prospectively include up to 10,000 patients visiting the hospital for elective major surgery. Data defining participants demographics, medical history and questionnaire data will be collected and stored in dedicated databases. Additional details (surgery and perioperative management, pain processing phenotypes and surgical and pain outcomes) will be stored.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Ages 18 - 80 years, consenting, planned surgery, able to understand and answer questionnaires.

Exclusion Criteria

  • •Non-consent, inability to give consent, unplanned and emergency surgery.

Outcomes

Primary Outcomes

Genetic risk factors for the development of acute pain using a visual analogue scale.

Time Frame: 7 days

All patients will be followed for 1 year after elective surgery, during this period the investigators will collect acute pain measures using a visual analogue scale (ranging from 0 (no pain) -10 (pain)) before the operation and 1, 2, 3 and 7 days after the operation.

Genetic risk factors for the development of chronic pain (defined as pain (yes or no) for more than 3 months in one specific body area).

Time Frame: 6 months

All patients will be followed for 1 year after elective surgery, during this period the investigators will collect chronic pain measures using a questionnaire before the operation and 1 week, 3 months and 6 months. Chronic pain is defined as pain at a specific body side (yes/no) for more than 3 months.

Secondary Outcomes

  • If the pain influences daily functioning will be assesed with the pain disability index.(6 months)
  • Is fear before an operation related to the development of acute and chronic pain after the operation.(once pre-operatively)
  • Is the Pain Catastrophizing Scale related to the development of acute and chronic pain after the operation.(once pre-operatively)
  • Is days in hospital after the operation associated with pain development.(6 months)
  • Is the size of the incision made during the operation associated with pain development.(6 months)
  • Is Pain Sensitivity related to the development of acute and chronic pain after the operation.(once pre-operatively)
  • Is medication use after the operation assocaited with pain development.(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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