Post Operative Pain Clinical Trial
Official title:
Postoperative Pain: Is Tunneling Effective in Preventing Failure of Epidural Analgesia? A Randomized Trial
This is a prospective randomized single blinded study in patients planned to undergo general
anesthesia and epidural catheter insertion for pain control after abdominal, thoracic and
orthopedic surgery.
Patients meeting participation criteria will be selected and enrolled sequentially.
The study recruitment will be carried out over one year with follow-up for each patient until
either the catheter is dislodged or once decided that the patient is to be discontinued from
the epidural pain control.
Study Population and Sample Size The study aims to enroll 200 adult patients planned to
undergo general anesthesia and epidural catheter insertion. The study sample will be selected
to fulfill the selection criteria.
Patients will be selected if they meet the following participation criteria:
Planned Procedures and Assessments Follow -up on dislodgments, adverse events, pain and pain
relief assessment, standard practice Study Site All study conduction from start to end
including procedures and assessments, data acquisition and analysis and final study
conclusion report and any publications will be at King Hussein Cancer Center (KHCC).
Ethical Considerations The study will be submitted to the KHCC IRB for review. The study will
not start before IRB approval is obtained.
All patients who provide consent to participation in the study will be randomized and
enrolled.
Statistical Plan Descriptive statistics will be used to present the two groups baseline
characteristics. Comparison between groups will be carried out using Chi-square test or
t-test or Wilcox on rank test as appropriate. Comparison between groups while adjusting for
other variables will be carried out using logistic regression. Odds ratios along with their
95% confidence intervals will be calculated.
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