Optimal Perioperative Pain Control in Minimally Invasive Abdominal Cancer Surgery

This is a research study to evaluate the effectiveness of 3 different types of routine pain management regimens used during clinically indicated, minimally invasive oncologic (cancer) surgery. This project is considered "Research" and participation is voluntary. Upon enrollment in this study, the research team will collect data from the patient's medical records. The patient will undergo all of the normal testing and procedures required pre-operatively (standard of care). The study team will then randomly assign the patient (like a flip of a coin) to one of three different study arms for pain

Trial Details

NCT ID
NCT06731998
Phase
NA
Sponsor
Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
Status
RECRUITING
Cancer Type
Pancreatic Cancer
Interventions
  • Local Anesthesia
  • Laparoscopic Transversus Abdominis Plane block
Locations (sample)
  • Pittsburgh, Pennsylvania, United States|40.44062,-79.99589

Key Eligibility Criteria

  • Male and female patients age ≥ 18 - 89
  • Patients scheduled for elective (clinically indicated) hepatic, gastric, biliary, pancreatic, gynecologic, colorectal, other GI Minimally invasive …
  • Patients who have provided informed consent to participate in the study.
  • Patients with an American Society of Anesthesiologists (ASA) physical status classification of I, II, or III.

For full eligibility, visit ClinicalTrials.gov.

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