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Last Updated: October 21, 2019

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CLINICAL TRIALS PROFILE FOR OFIRMEV

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Clinical Trials for Ofirmev

Trial ID Title Status Sponsor Phase Start Date Summary
NCT01500109 Efficacy of Oral Versus Intravenous Acetaminophen for Primary Pediatric Cleft Palate Repair Completed Loma Linda University N/A 2011-11-01 The purpose of this investigator-initiated study is to determine whether acetaminophen is an effective pain reliever for primary cleft palate repair in children and possesses opioid sparing effects. Additionally, the investigators will determine if patients who receive acetaminophen have less opioid related side-effects. The study will have three study groups based on whether the patient receives Ofirmev® and opioids (Fentanyl and Morphine), oral acetaminophen elixir and opioids (Fentanyl and Morphine), or opioids (Fentanyl and Morphine) alone. Total opioid (Fentanyl and Morphine) consumption will be tracked for the intraoperative period and 24 hours after surgery for all patients within the study and converted to morphine equivalents.
NCT01520298 Intravenous Acetaminophen as Adjuvant Therapy for Pain Control in Geriatric Hip Fracture Patients Withdrawn Lancaster General Hospital Phase 3 2011-12-01 This research study is a prospective, randomized, blinded, placebo controlled trial evaluating the benefit of IV acetaminophen (Ofirmev™) as adjuvant analgesia in geriatric hip fracture patients. IV acetaminophen has received FDA approval. IV acetaminophen does not have the liver toxicity as oral acetaminophen. No oral acetaminophen will be administered. All patients diagnosed with a hip fracture aged at least 65 years and expected to undergo surgical intervention are eligible to participate. Hip fractures affect greater than 300,000 geriatric patients annually, representing the second leading cause of hospitalization for this patient population. Pain control in these patients is often problematic due to co-morbidities and changes in their pharmacokinetic and pharmacodynamic profiles. Subjects may receive the normal DVT prophylactic treatments post-op.
NCT01544062 IV Acetaminophen as an Adjunct Analgesic in Cardiac Surgery Completed Mallinckrodt Phase 4 2012-07-01 Patients undergoing cardiac surgery experience significant postoperative pain, which may impact postoperative outcomes. The aim of this single center, double-blind, randomized, placebo controlled trial is to determine if intravenous (IV) acetaminophen will significantly decrease 24 hour postoperative opioid consumption.
NCT01544062 IV Acetaminophen as an Adjunct Analgesic in Cardiac Surgery Completed University of Washington Phase 4 2012-07-01 Patients undergoing cardiac surgery experience significant postoperative pain, which may impact postoperative outcomes. The aim of this single center, double-blind, randomized, placebo controlled trial is to determine if intravenous (IV) acetaminophen will significantly decrease 24 hour postoperative opioid consumption.
NCT01598701 Intravenous Acetaminophen in Craniotomy Active, not recruiting Mallinckrodt Phase 4 2012-06-01 The purpose of this study is to assess the use of intravenous Acetaminophen (OFIRMEV) as an effective adjunct therapeutic agent in patients undergoing craniotomy.
NCT01598701 Intravenous Acetaminophen in Craniotomy Active, not recruiting The University of Texas Health Science Center, Houston Phase 4 2012-06-01 The purpose of this study is to assess the use of intravenous Acetaminophen (OFIRMEV) as an effective adjunct therapeutic agent in patients undergoing craniotomy.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Ofirmev

Condition Name

Condition Name for Ofirmev
Intervention Trials
Pain 7
Pain, Postoperative 5
Postoperative Pain 5
Acute Pain 3
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Condition MeSH

Condition MeSH for Ofirmev
Intervention Trials
Pain, Postoperative 17
Acute Pain 4
Vomiting 2
Fractures, Bone 2
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Clinical Trial Locations for Ofirmev

Trials by Country

Trials by Country for Ofirmev
Location Trials
United States 42
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Trials by US State

Trials by US State for Ofirmev
Location Trials
New York 9
Ohio 6
Texas 5
Florida 4
Pennsylvania 4
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Clinical Trial Progress for Ofirmev

Clinical Trial Phase

Clinical Trial Phase for Ofirmev
Clinical Trial Phase Trials
Phase 4 33
Phase 3 6
Phase 2 3
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Clinical Trial Status

Clinical Trial Status for Ofirmev
Clinical Trial Phase Trials
Recruiting 15
Not yet recruiting 11
Completed 9
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Clinical Trial Sponsors for Ofirmev

Sponsor Name

Sponsor Name for Ofirmev
Sponsor Trials
Mallinckrodt 11
Beth Israel Deaconess Medical Center 2
Florida Hospital 2
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Sponsor Type

Sponsor Type for Ofirmev
Sponsor Trials
Other 49
Industry 13
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Serving leading biopharmaceutical companies globally:

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