Acute Pancreatitis
Conditions
Brief summary
Acute pancreatitis is a painful and potentially life-threatening condition that affects the pancreas, a glandular organ responsible for producing digestive enzymes and hormones. The condition is typically characterized by sudden inflammation of the pancreas that can cause severe abdominal pain, nausea, and vomiting. Treatment for acute pancreatitis usually involves supportive care, pain management, and sometimes, hospitalization. Nonsteroidal anti-inflammatory drugs (NSAIDs) and opioids are two of the most commonly used classes of pain medication for the management of acute pancreatitis. While both drugs are effective in reducing pain, they have different mechanisms of action and potential side effects. NSAIDs work by reducing inflammation and pain by inhibiting the activity of cyclooxygenase (COX) enzymes, whereas opioids work by binding to specific receptors in the brain and spinal cord to block the transmission of pain signals. Despite their widespread use, there is a lack of consensus regarding which medication is more effective for the management of acute pancreatitis, particularly in mild to moderate cases. Some studies have suggested that NSAIDs may be more effective for reducing pain in acute pancreatitis, while others have suggested that opioids may be more effective in providing pain relief. Moreover, there is a concern regarding the potential for adverse events associated with the use of opioids, such as respiratory depression, addiction, and constipation. Therefore, this study aims to compare the efficacy and safety of NSAIDs and opioids in the management of mild to moderate acute pancreatitis. This will be a randomized clinical trial, which will involve the recruitment of patients with mild to moderate acute pancreatitis who will be randomized to receive either an NSAID or an opioid for pain management. The primary outcome of this study will be the reduction in pain score measured using a visual analogue scale (VAS) over a 72-hour period. The secondary outcomes will include adverse events associated with each medication, length of hospital stay, and the need for further interventions. This study has the potential to provide important insights into the optimal management of pain in mild to moderate acute pancreatitis, which can ultimately improve patient outcomes and reduce the burden of this condition on the healthcare system.
Interventions
DRUGKetorolac
Injection ketorolac 30 mg IV x TDS will be given to each patient in each group.
DRUGTramadol
Injection Tramadol 25-50 mg IV x TDs wil be given to each patient in this group. Maximum dose will be 400 mg/ day
Sponsors
Hayatabad Medical Complex
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Age 18 years or older * Diagnosis of mild to moderate acute pancreatitis based on clinical and radiological criteria * Moderate pain intensity (NRS score of 4-7) * No history of allergy or intolerance to NSAIDs or opiates * No history of opioid abuse or addiction
Exclusion criteria
* Severe acute pancreatitis requiring intensive care unit admission * Pregnancy or lactation * History of significant renal or hepatic dysfunction * Use of non-steroidal anti-inflammatory drugs or opiates in the past 24 hours * Known or suspected peptic ulcer disease * Known or suspected gastrointestinal bleeding * Participation in another clinical trial in the past 30 days * Inability to provide informed consent * Inability to communicate pain intensity using the numeric rating scale * Allergy or intolerance to any of the study medications or their components.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain Intensity at 2 hours | 2 hours | The numeric rating scale (NRS) is a pain screening tool, commonly used to assess pain severity at that moment in time using a 0-10 scale, with zero meaning no pain and 10 meaning the worst pain imaginable. The primary outcome of this study is pain intensity measured on the NRS at 2 hours after the intervention |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pain intensity at 4, 6, 8, and 24 hours after the intervention | 4-24 hours | The numeric rating scale (NRS) is a pain screening tool, commonly used to assess pain severity at that moment in time using a 0-10 scale, with zero meaning no pain and 10 meaning the worst pain imaginable. Pain intensity will be measured at NRS scale at 4, 6, 8 and 24 hours after the intervention and recorded accordingly |
| time to pain relief | 0-24 hours | How much time did it take for the pain to relieve completely. (In hours) |
| adverse events | 0-24 hours | any adverse events with the drug intervention will be noted |
| patient satisfaction with pain management. | 1 day | In this study, patient satisfaction with pain management will be assessed using a modified version of the Likert scale. Participants will be asked to rate their satisfaction with pain management on a scale from 1 to 5, where 1 is very dissatisfied, 2 is somewhat dissatisfied, 3 is neither satisfied nor dissatisfied, 4 is somewhat satisfied, and 5 is very satisfied. This scale will be administered at 24 hours after the intervention. The satisfaction scale will also include an open-ended question to allow patients to provide any comments or suggestions regarding their pain management experience. These comments can provide valuable insights into the patient experience and help to inform future pain management practices. |
Countries
Pakistan
Contacts
Primary ContactMusarrat Hussain
Backup ContactMuhammad Jawad Zahid
Outcome results
None listed