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.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05619796 -
Assessment of Clinical & Radiographic Efficiency of Manual & Pediatric Rotary Systems in Primary Root Canal Preparation
|
N/A | |
Recruiting |
NCT05338671 -
Effect of Post-Operative Anesthetics on Post-Operative Pain in Patients Receiving Endodontic Treatment
|
Phase 4 | |
Completed |
NCT05584696 -
Effectiveness of Green Color Exposure on Dental Anxiety
|
N/A | |
Completed |
NCT05593341 -
Opioid Education in Total Knee Arthroplasty
|
N/A | |
Not yet recruiting |
NCT05255146 -
Cryoanalgesia and Post-thoracotomy Pain in Minimally Invasive Cardiothoracic Surgery
|
N/A | |
Not yet recruiting |
NCT06020196 -
The Safety and Efficacy of Surgical Rectus Sheath Block for Postoperative Analgesia After Elective Cesarean Delivery
|
N/A | |
Completed |
NCT01697748 -
Prospective Study on Cesarean Wound Outcomes
|
N/A | |
Completed |
NCT01681966 -
A Single-dose Open-Label Study to Assess the Safety and Preliminary Efficacy of PRF 110 in Open Herniorrhaphy Surgery
|
Phase 2 | |
Completed |
NCT01442818 -
Patient Satisfaction and Pain Control Following Reconstructive Vaginal Surgery
|
N/A | |
Completed |
NCT00625911 -
Ketamine Improves Post-Thoracotomy Analgesia
|
N/A | |
Terminated |
NCT05494125 -
Effects of Continuous ESP Catheters on Recovery, Pain and Opioid Consumption After Multilevel Spine Surgery
|
N/A | |
Recruiting |
NCT04767399 -
Comparison of Postoperative Pain After Instrumentation in Different Visits With Different Single File Systems.
|
N/A | |
Not yet recruiting |
NCT05863624 -
Open and Endoscopic Technique in Female Inguinal Hernia Repair. FemaleHernia
|
N/A | |
Completed |
NCT06048744 -
Ultrasound Guided Erector Spinae Plane Block vs External Oblique Intercostal Plane Block for Nephrectomy
|
N/A | |
Active, not recruiting |
NCT05374499 -
Double-Blinded Randomized Controlled Study Investigating the Efficacy of Exparel (Liposomal Bupivacaine) for Postoperative Pain Relief in Mandibular Third Molar Extractions
|
Phase 4 | |
Completed |
NCT05552391 -
Dexametomedine Versus Ketamine as an Adjuvant in Erector Spinae Block for Perioperative Thoracotomy Pain Control
|
Phase 4 | |
Completed |
NCT05510947 -
Acute Postoperative Pain and Catastrophizing in Patients Undergoing Unicompartmental Knee Arthroplasty
|
||
Completed |
NCT06065683 -
Acute Postoperative Pain Prevalence and Intensity in the First 72 Hours
|
||
Completed |
NCT06082479 -
The Effect of Intra Oral Cryotherapy in Patients With Symptomatic Apical Periodontitis
|
N/A | |
Recruiting |
NCT04909060 -
Does the Newborn Infant Parasympathetic Evaluation (NIPE) Index Predict Postsurgical Pain in Children
|