Media Articles Related to Oxycodone and Aspirin (Oxycodone / Oxycodone / Aspirin)
A 48-Year-Old Man With Abdominal Pain and Vomiting: Osmosis USMLE Study Question of the Week
Source: Medscape Medical Students Headlines [2017.01.20]
A 48-year-old man presents with recurrent abdominal pain and vomiting. Which enzyme is likely affected?
Treating Chronic Pain in Patients With Prior Opioid Abuse
Source: Medscape Anesthesiology Headlines [2017.01.19]
Are we being overly cautious in treating patients with prior opioid abuse for chronic pain?
Key signaling protein associated with addiction controls the actions of oxycodone on pain
Source: Pain / Anesthetics News From Medical News Today [2017.01.19]
RGS9-2, a key signaling protein in the brain known to play a critical role in the development of addiction-related behaviors, acts as a positive modulator of oxycodone reward in both pain-free and...
Source: MedicineNet Ankle Pain and Tendinitis Specialty [2017.01.19]
Title: Leg Pain
Category: Symptoms and Signs
Created: 12/3/2009 12:00:00 AM
Last Editorial Review: 1/19/2017 12:00:00 AM
Forward-Thinking Tips for Back Pain
Source: MedicineNet Depression Specialty [2017.01.19]
Title: Forward-Thinking Tips for Back Pain
Category: Health News
Created: 1/18/2017 12:00:00 AM
Last Editorial Review: 1/19/2017 12:00:00 AM
Published Studies Related to Oxycodone and Aspirin (Oxycodone / Oxycodone / Aspirin)
Oxycodone-related side effects: impact on degree of bother, adherence, pain relief, satisfaction, and quality of life. [2011.05]
OBJECTIVES: Oxycodone immediate-release, alone or in combination (hereafter, oxycodone), is widely used to treat pain and is often associated with bothersome side effects. The objective was to assess side effect frequency, degree of bother, and impact on health-related quality of life (HRQoL)... CONCLUSIONS: The majority of survey respondents experienced side effects of oxycodone, with a majority being bothered by side effects and impacting their QoL. This raises a question about the unmet need for pain medications with improved side effect profiles.
Oxycodone combinations for pain relief. [2010.06]
No single analgesic drug provides the perfect therapeutic/adverse effect profile for every pain condition. In addition to convenience and possibly improved compliance, a combination of analgesic drugs offers the potential, requiring verification, of providing greater pain relief and/or reduced adverse effects than the constituent drugs when used individually...
Clinical Trials Related to Oxycodone and Aspirin (Oxycodone / Oxycodone / Aspirin)
Early Postoperative Administration of Oxycodone +/- Naloxone and Duration of Epidural Analgesia [Not yet recruiting]
Cystectomy with urinary diversion (ileal conduit, ileal orthotopic neobladder,
catheterizable ileal pouch) is major abdominal surgery, which is associated with a high
incidence of gastrointestinal complications. Perioperative techniques aiming at an early
return of bowel function are to be pursued.
Optimal postoperative pain management is one of the key factors leading to enhanced recovery
after surgery. The perioperative use of an epidural analgesia for major abdominal surgery is
established, not only because of its excellent analgesic properties, but also because it can
accelerate the return of bowel function. However, epidural analgesia is associated with
additional costs, need for close monitoring and nursing. In addition each supplemental day
with an indwelling epidural catheter increases the risk of infection. So it is recommended
to re-assess the risk/benefit ratio of an epidural analgesia after 4 days, if not sooner.
Therefore, it is important to develop strategies that reduce its duration without impairing
the benefits. Systemic analgesics with prolonged-release oral formulation like oral
oxycodone (OxycontinÂ®) or combined drug mixture (oral oxycodone/naloxone (TarginÂ®)) could be
a valuable alternative pain treatment as a second analgesic step, starting on postoperative
day (POD) 3, so that the epidural catheter could be removed earlier without impairing
postoperative enhanced recovery including return of the bowel function. Both oxycodone and
naloxone orally administered are a recognized and accepted treatment option.
The objective of this study is to evaluate the implementation of an oral opioid with or
without naloxone in the early postoperative period in patients undergoing open radical
cystectomy with urinary diversion and intraoperative and early postoperative use of epidural
analgesia. The investigators expect an unchanged early return of the bowel function and
equal analgesia with a reduced length of stay of the epidural catheter (primary endpoint),
thus potentially reducing epidural catheter associated complications and lowering costs
(nursing and pain service).
Pharmacokinetics And Relative Bioavailability Study Of Oxycodone [Completed]
Abuse Liability of Controlled-Release Oxycodone Formulations [Completed]
The objective of this study is to examine the abuse liability of a single 40mg dose of 2
controlled release oxycodone formulations (Apo-Oxycodone CR® and OxyNEO®) in non-dependent
recreational opioid users by assessing the self-reported acute effects of the drugs and
taking blood samples to measure drug concentrations. The investigators think there may be
differences in how well these drugs are liked when swallowed whole due to differences in how
the products are formulated.
Comparison of the Efficacy of Oral Oxycodone and Oral Codeine in the Treatment of Postcraniotomy Pain [Completed]
The efficacy of codeine is dependent on its demethylation to morphine. This extent of
demethylation has wide inter-individual variability, making codeine's efficacy as a
analgesic variable. Oxycodone is a semi-synthetic opioid and is a weak agonist on mu opioid
Codeine has been the mainstay of analgesia for patients after craniotomy for many years.
Traditionally, craniotomies were not thought to be very painful procedures, hence the use of
codeine, a moderately potent opioid (when compared to morphine).
However, in recent years, it has been found that up to 70% of post-craniotomy patients have
moderate to severe pain and codeine did not provide adequate analgesic relief. Many studies
have compared codeine to other drugs such as PCA morphine, fentanyl and tramadol, and
patients on these stronger opioids generally had lower pain scores and better satisfaction.
No study has been conducted to determine the efficacy of analgesia of oral oxycodone to oral
Hence, the hypothesis is that oxycodone is more effective than codeine in providing pain
relief in post-craniotomy patients.
Comparison of the Effects of Tapentadol and Oxycodone on Gastrointestinal and Colonic Transit in Humans [Completed]
Tapentadol is FDA approved for the treatment of moderate to severe acute pain. Due to the
dual mechanism of action as an opioid agonist and norepinephrine reuptake inhibitor, there
is potential for off label use in chronic pain.
Tapentadol is a new molecular entity that is structurally similar to tramadol. Tapentadol
is a centrally-acting analgesic with a dual mode of action as an agonist at the mu-opioid
receptor and as a norepinephrine reuptake inhibitor. These two actions are synergistic in
pain relief. While its action reflects aspects of tramadol and morphine, its ability to
control pain is more on the order of hydrocodone and oxycodone.
Its dual mode of action provides analgesia at similar levels of more potent narcotic
analgesics such as hydrocodone, oxycodone, and meperidine with a more tolerable side effect
profile. Clinical studies showed that tapentadol effectively relieves moderate to severe
pain in various pain care settings. In addition, it was reported to be associated with
significantly fewer treatment discontinuations due to a significantly lower incidence of
gastrointestinal-related adverse events compared with equivalent doses of oxycodone. The
combination of these reduced treatment discontinuation rates and tapentadol efficacy for the
relief of moderate to severe nociceptive and neuropathic pain may offer an improvement in
pain therapy by increasing patient compliance with their treatment regimen.