Postoperative PainPhase 2NCT00831051
Comparison of the Efficacy and Safety of Q8003 Versus Its Individual Components in Bunionectomy Patients
A Phase 2 study testing Q8003, Morphine sulfate and Oxycodone HCl in people with Postoperative Pain, run by QRxPharma Inc. at 6 sites in United States.
Trial summary
This is a randomized, double-blind, multicenter, fixed dose factorial study of Q8003 12 mg/8 mg and Q8003 6 mg/4 mg versus its individual morphine sulfate and oxycodone hydrochloride components for the management of acute moderate to severe postoperative pain following bunionectomy surgery. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Postoperative Pain
- What is being tested?
- Q8003, Morphine sulfate and Oxycodone HCl
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 197 participants
- Where
- 6 sitesUnited States
- Study dates
- Dec 2008to Feb 2009
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patient is male or female and at least 18 years of age.
- Females must be non-pregnant, non-lactating, and practicing an acceptable method of birth control, or be surgically sterile or postmenopausal (amenorrhea for ≥ 12 months). Non-pregnancy will be confirmed by pregnancy tests conducted at Screening and Pre-treatment.
- Patient is scheduled for bunionectomy surgery, meets the criteria of an ASA Class I to III, and is willing to stay in the study center for at least 48 hours from the initial dose of study medication post surgery.
- To be randomized after surgery, the patient must report moderate to severe pain (a score of 2 or more on the 4 point Likert scale or at least 4 on the 11 point NPRS scale).
Who cannot join
- In the opinion of the Investigator, has a history of pulmonary, cardiovascular (including uncontrolled hypertension), neurologic, endocrine, hepatic, gastrointestinal, or kidney disease or therapy that, in the opinion of the Investigator, would jeopardize the patient's well being by participation in this study or is mentally or emotionally unsuitable to participate, or unable/unwilling to comply with the study assessments.
- Used opiates continuously (including tramadol) for more than ten days in the past year.
- Hypersensitivity or poor tolerance to ibuprofen or short term opioids.
- Currently receiving any medications that are not at a stable dose (the same dose for > 2 months prior to date of surgery).
- Was dosed with another investigational drug within 30 days prior to the Screening Visit or has previously received treatment with Q8003.
- Current therapy with central nervous system depressant medications that might increase the risks of treatment with opioids (other than those used with surgical anesthesia).
- Current evidence of alcohol abuse (regularly drinks more than 4 units of alcohol per day; 1 unit = ½ pint of beer, 1 glass of wine, or 1 ounce of spirit).
Trial locations and contacts
6 sites in 1 country.
6 sites in 1 country
United States6 sites
Advanced Regional Center for Ankle and Foot Care
Altoona, Pennsylvania, 92801
Advanced Clinical Research Institute
Anaheim, California, 92801
Crossroads Research, Inc.
Owings Mills, Maryland, 21117
Chesapeake Foot and Ankle
Pasadena, Maryland, 21122
Associated Foot and Ankle Specialists
Phoenix, Arizona, 85050
Jean Brown Research
Salt Lake City, Utah, 84124
About this study
Official title: A Double-Blind, Randomized, Multi-Center, Repeat-Dose, Comparison of the Analgesic Efficacy and Safety of the Opioid Combination Q8003 to Each of the Individual Milligram Components (Oxycodone and Morphine) in the Management of Acute Moderate to Severe Pain Following Bunionectomy Surgery
This is a randomized, double-blind, multicenter, fixed dose factorial study of Q8003 12 mg/8 mg and Q8003 6 mg/4 mg versus its individual morphine sulfate and oxycodone hydrochloride components for the management of acute moderate to severe postoperative pain following bunionectomy surgery.
- Conditions
- Postoperative Pain
- Being tested
- Q8003, Morphine sulfate, Oxycodone HCl, Oxycodone HCl 4mg
- Keywords
- Bunionectomy
- Medical subject headings
- Pain, Postoperative
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Q8003Drug
One Q8003 (morphine sulfate and oxycodone HCl) 12mg/8mg IR Capsule q6h
Morphine sulfateDrug
One morphine sulfate 12mg IR capsule q6h
Oxycodone HClDrug
One oxycodone HCl 8mg IR Capsule q6h
Q8003Drug
One Q8003 (morphine sulfate and oxycodone HCl) 6mg/4mg IR Capsule q6h
Morphine sulfateDrug
Two morphine sulfate 3mg IR capsules q6h
Oxycodone HCl 4mgDrug
Two oxycodone HCl 2mg IR Capsules q6h
| Study group | Role | What they receive |
|---|---|---|
| Q8003 12mg/8mg | Experimental | Combination Receives: Drug: Q8003 |
| Morphine sulfate 12 mg | Active comparator | Single component Receives: Drug: Morphine sulfate |
| Oxycodone HCl 8mg | Active comparator | Single component Receives: Drug: Oxycodone HCl |
| Q8003 6mg/4mg | Experimental | Combination Receives: Drug: Q8003 |
| Morphine sulfate 6mg | Active comparator | Single component Receives: Drug: Morphine sulfate |
| Oxycodone HCl 4mg | Active comparator | Single component Receives: Drug: Oxycodone HCl 4mg |
What is being measured
The primary outcome is the main question the study is designed to answer.
Difference in pain intensity scores from baseline
Measured: 48 hours
Secondary outcomes (1)
Safety: adverse events
Measured: 48 hours
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Jan 2009 (estimated)
- Study startDec 2008
- Primary completionJan 2009
- Study completionFeb 2009
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Postoperative PainStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 197 participants (actual)
Sponsor and investigators
- Lead sponsor
- QRxPharma Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Patricia T. Richards, MD, Ph.D., Study director, QRxPharma Inc.
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00831051
- Sponsor's protocol ID
- Q8003-021
- Status last verified
- May 2012
- First submitted
- 27 Jan 2009
- Last updated
- 17 May 2012
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 May 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Double-Blind, Randomized, Multi-Center, Repeat-Dose, Comparison of the Analgesic Efficacy and Safety of the Opioid Combination Q8003 to Each of the Individual Milligram Components (Oxycodone and Morphine) in the Management of Acute Moderate to Severe Pain Following Bunionectomy Surgery
- ClinicalTrials.gov ID
- NCT00831051
- Acronym / sponsor ID
- Q8003-021
- Conditions
- Postoperative Pain
- Keywords
- Bunionectomy
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 197 participants (actual)
- Lead sponsor
- QRxPharma Inc.Industry (pharma, biotech, devices)
- Study start
- Dec 2008
- Primary completion
- Jan 2009 (actual)
- Study completion
- Feb 2009 (actual)
- First posted
- 28 Jan 2009 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a randomized, double-blind, multicenter, fixed dose factorial study of Q8003 12 mg/8 mg and Q8003 6 mg/4 mg versus its individual morphine sulfate and oxycodone hydrochloride components for the management of acute moderate to severe postoperative pain following bunionectomy surgery.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 6
| Arm | Type | Receives |
|---|---|---|
| Q8003 12mg/8mg | Experimental | Drug: Q8003Combination |
| Morphine sulfate 12 mg | Active comparator | Drug: Morphine sulfateSingle component |
| Oxycodone HCl 8mg | Active comparator | Drug: Oxycodone HClSingle component |
| Q8003 6mg/4mg | Experimental | Drug: Q8003Combination |
| Morphine sulfate 6mg | Active comparator | Drug: Morphine sulfateSingle component |
| Oxycodone HCl 4mg | Active comparator | Drug: Oxycodone HCl 4mgSingle component |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Patient is male or female and at least 18 years of age.
- Females must be non-pregnant, non-lactating, and practicing an acceptable method of birth control, or be surgically sterile or postmenopausal (amenorrhea for ≥ 12 months). Non-pregnancy will be confirmed by pregnancy tests conducted at Screening and Pre-treatment.
- Patient is scheduled for bunionectomy surgery, meets the criteria of an ASA Class I to III, and is willing to stay in the study center for at least 48 hours from the initial dose of study medication post surgery.
- To be randomized after surgery, the patient must report moderate to severe pain (a score of 2 or more on the 4 point Likert scale or at least 4 on the 11 point NPRS scale).
Key exclusion criteria (7 listed)
- In the opinion of the Investigator, has a history of pulmonary, cardiovascular (including uncontrolled hypertension), neurologic, endocrine, hepatic, gastrointestinal, or kidney disease or therapy that, in the opinion of the Investigator, would jeopardize the patient's well being by participation in this study or is mentally or emotionally unsuitable to participate, or unable/unwilling to comply with the study assessments.
- Used opiates continuously (including tramadol) for more than ten days in the past year.
- Hypersensitivity or poor tolerance to ibuprofen or short term opioids.
- Currently receiving any medications that are not at a stable dose (the same dose for > 2 months prior to date of surgery).
- Was dosed with another investigational drug within 30 days prior to the Screening Visit or has previously received treatment with Q8003.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Q8003One Q8003 (morphine sulfate and oxycodone HCl) 12mg/8mg IR Capsule q6h | Drug | Q8003 12mg/8mg |
| Morphine sulfateOne morphine sulfate 12mg IR capsule q6h | Drug | Morphine sulfate 12 mg |
| Oxycodone HClOne oxycodone HCl 8mg IR Capsule q6h | Drug | Oxycodone HCl 8mg |
| Q8003One Q8003 (morphine sulfate and oxycodone HCl) 6mg/4mg IR Capsule q6h | Drug | Q8003 6mg/4mg |
| Morphine sulfateTwo morphine sulfate 3mg IR capsules q6h | Drug | Morphine sulfate 6mg |
| Oxycodone HCl 4mgTwo oxycodone HCl 2mg IR Capsules q6h | Drug | Oxycodone HCl 4mg |
Primary outcome
Difference in pain intensity scores from baseline
Time frame: 48 hours
1 secondary outcome
Safety: adverse events
Time frame: 48 hours
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 May 2012.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Patricia T. Richards, MD, Ph.D. study director
QRxPharma Inc.
6 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Q8003, Morphine sulfate and Oxycodone HCl in people with Postoperative Pain, run by QRxPharma Inc. at 6 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 17 May 2012. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 6 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Difference in pain intensity scores from baseline (time frame: 48 hours). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 May 2012.