Trial of Caldolor for Treatment of Pain in Post-Operative Adult Patients

Completed · Phase 3 · Has a placebo group

Conditions studied: Pain

In brief

The primary objective of this study of Caldolor (IV ibuprofen) administered to post-operative hospitalized adult patients every 6 hours for 48 hours is to determine the efficacy of Caldolor compared to placebo for the treatment of post-operative pain as measured by reduction in the requirement for the narcotic analgesic, morphine, post surgery

Key facts

Study ID

NCT00225732

Run by

Cumberland Pharmaceuticals

People needed

319

Starts

2005-01-01

Expected to finish

2008-01-01

Last updated by the study team

2016-06-22

Who can join

Age: 18 and older, up to 70. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Scheduled for elective abdominal hysterectomy surgery with anticipated need for post-operative I.V. morphine analgesia with anticipated use of ≥ 24 hours.
• Adequate IV access
• Anticipated hospital stay ≥ 24 hours

You may not qualify if…

• Be unable to make a reliable self-report of pain intensity to pain relief
• Less than 18 years of age
• Greater than 70 years of age
• Use of NSAIDs within 12 hours prior to dosing
• Use of analgesics, muscle relaxants and sedatives less than 24 hours prior to CTM administration with the following exceptions: paracetamol (acetaminophen) can be administered until 6 hours prior to surgery; tramadol can be administered until midnight the evening prior to surgery; muscle relaxants working at the neuromuscular junction used for intubation and/or anesthesia administration for the surgical procedure prior to CTM administration; and sedatives (i.e., midazolam) used as a co-induction agent for the surgical procedure prior to CTM administration
• Patients taking warfarin, lithium, combination of ACE-inhibitors and furosemide
• Patients with anemia (active clinically significant) and/or a history or evidence of asthma or heart failure
• History of allergy or hypersensitivity to any component of Caldolor, aspirin (or aspirin related products), NSAIDs, or COX-2 inhibitors
• Pregnant or nursing
• History of severe head trauma that required current hospitalization, intracranial surgery or stroke within the previous 30 days, or any history of intracerebral arteriovenous malformation, cerebral aneurysm or CNS mass lesion
• Weigh less than 30kg
• Have a history of congenital bleeding diathesis (eg hemophilia) or any active clinically significant bleeding, or have underlying platelet dysfunction including (but not limited to) idiopathic thrombocytopenic purpura, disseminated intravascular coagulation, or congenital platelet dysfunction
• Have GI bleeding that required medical intervention within the previous 6 weeks (unless definitive surgery has been performed)
• Have a platelet count less than 30,000mm3 determined within the 28 days prior to surgery
• Pre-existing dependence on narcotics or known tolerance to opioids
• Inability to understand the requirements of the study, be willing to provide written informed consent (as evidenced by signature on an informed consent document approved by an Institutional Review Board [IRB]), and agree to abide by the study restrictions and to return for the required assessments
• Refusal to provide written authorization for use and disclosure of protected health information
• Be on dialysis, have oliguria or calculated creatinine clearance of less than 60 mL/min (calculated using the Cockcroft and Gault formula) determined within the 28 days prior to surgery
• Inability to achieve hemostasis or inability to close surgical incision, prior to Operating Room discharge
• Operative procedure includes organ transplant
• Pre or intra-operative procedure utilized for the prevention of pre- or post-operative pain (i.e. epidural or nerve blocks)
• Be receiving full dose anticoagulation therapy or Activated Protein C within 6 hours before dosing (Prophylaxis with subcutaneous heparin is acceptable)
• Have received another investigational drug within the past 30 days
• Be otherwise unsuitable for the study in the opinion of the investigator

Where it is running

• Cooper Green Hospital / Jefferson Clinic — Birmingham, Alabama, United States
• Medical Center East / Alabama Clinical Therapeutics — Birmingham, Alabama, United States
• Springhill Hospital / Wilmax Clinical Research, Inc. — Mobile, Alabama, United States
• Mobile Infirmary Medical Center / Wilmax Clinical Research, Inc. — Mobile, Alabama, United States
• Jackson Hospital / Drug Research and Analysis Corporation — Montgomery, Alabama, United States
• Baptist Medical Center South / Drug Research and Analysis Corporation — Montgomery, Alabama, United States
• Arizona Research Center — Phoenix, Arizona, United States
• Valley OB/GYN — Colton, California, United States
• Research Support Personnel LLC — Wichita, Kansas, United States
• Chandler Medical Center; Ken Muse Research — Lexington, Kentucky, United States
• Comprehensive Pain Specialists — Hendersonville, Tennessee, United States
• Health First Medical Group — Fort Worth, Texas, United States
• Royal Adelaide Hospital — Adelaide, Australia

Full record on ClinicalTrials.gov

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