Clinical Trial

Analgesic Effect of Parecoxib Versus Morphine in SCD Patients Presenting to the Emergency Department

Study acronym: PASC
Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
Introduction: This study focuses on the treatment of painful crises in Sickle Cell Disease (SCD) patients using Paracoxib, a non-opioid, compared to Morphine. It addresses the need for alternative medications that reduce opioid dependency while providing effective analgesia. Objectives: Primary: Evaluate the analgesic effect of Paracoxib versus Morphine in SCD vaso-occlusive crises. Secondary: Reduce opioid use/dependence, decrease the length of hospital stays, and monitor side effects related to Paracoxib. Methodology: A double-blinded randomized controlled trial, conducted in a tertiary care emergency department. The study includes adult SCD patients with moderate to severe crises, excluding non-VOC pain, certain medications, and specific medical conditions. The sample size is 226 patients, split equally into two groups. Intervention: Patients receive either Morphine or Paracoxib, with periodic assessment of vital signs and pain. Additional Morphine is administered if required. Data collection and analysis are meticulously planned. Expected Outcomes: Improvement in SCD pain management, reduction in opioid usage, and potential benefits in terms of hospital stays and patient satisfaction.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-03-12.
Trial Details
NCT Number NCT06315920
Lead Sponsor Oman Medical Speciality Board
Collaborators: Armed Forces Hospital, Oman
Conditions Sickle-Cell Disease with Crisis
Enrollment 226 participants
Start Date 2026-05-01
Primary Completion 2028-05-01 (estimated)
Study Completion 2028-07-01 (estimated)
Updated on ClinicalTrials.gov 2025-03-20