Remifentanil vs Fentanyl During Cardiac Surgery and Chronic Thoracic Pain
Information source: St. Antonius Hospital
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Chronic Pain; Sternotomy; Remifentanil; Fentanyl
Intervention: Fentanyl (Drug); Remifentanil (Drug); Fentanyl (Drug)
Phase: Phase 4
Status: Recruiting
Sponsored by: St. Antonius Hospital Official(s) and/or principal investigator(s): CAJ Knibbe, Prof. Dr., Principal Investigator, Affiliation: St. Antonius Hospital
Overall contact: S. de Hoogd, MSc, Phone: +3130-6093500, Email: s.de.hoogd@antoniusziekenhuis.nl
Summary
This study will investigate the influence of intra-operative use of remifentanil versus
fentanyl on the percentage of patients with chronic thoracic after cardiac surgery via
sternotomy. Secondary quantitative sensory testing is performed to determine thermal and
electrical detection and pain threshold and the difference in pain variability scoring.
Postoperative pain scores, analgesic use, genetic variances and costs are measured.
Clinical Details
Official title: A Randomised Clinical Trial Evaluating the Effect of Remifentanil vs Fentanyl During Cardiac Surgery on the Incidence of Chronic Thoracic Pain
Study design: Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention
Primary outcome: Chronic thoracic pain
Secondary outcome: Chronic thoracic painMean Numerical Rating Scale (NRS) score Quality of life Thermal detection and pain thresholds Pain variability Use of analgesics during and after hospitalization Genetic variances Total medical costs and productivity costs during one year, including costs of hospitalization days (ICU and non-ICU) and costs of medications Mean pain NRS (Numerical Rating Scale)
Eligibility
Minimum age: 18 Years.
Maximum age: 85 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Patients undergoing cardiac surgery via sternotomy (Coronary artery bypass graft
(CABG) and/or valve replacement)
- Patients admitted to the ICU or PACU in the St. Antonius hospital
- Patients between 18 and 85 years old
- Patients weighing between 45 and 140 kg
- Written informed consent
Exclusion Criteria:
- Pregnancy/ breastfeeding
- Language barrier
- History of drug abuse
- Neurologic condition such as peripheral neuropathy
- Known remifentanil, fentanyl, morphine or paracetamol allergy
- Body Mass Index (BMI) > 35 kg/m2
- Prior cardiac surgery (re-operations);
- Patients with chronic pain conditions.
Locations and Contacts
S. de Hoogd, MSc, Phone: +3130-6093500, Email: s.de.hoogd@antoniusziekenhuis.nl
St. Antonius Hospital, Nieuwegein, Netherlands; Recruiting S. de Hoogd, MSc., Phone: +3130-6093500, Email: s.de.hoogd@antoniusziekenhuis.nl
Additional Information
Starting date: February 2014
Last updated: October 30, 2014
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