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CompletedNCT00784277Updated Feb 13, 2012Results posted

A Study to Compare the Frequency of Constipation Symptoms With Tapentadol Immediate Release (IR) Treatment Versus Oxycodone IR Treatment in Patients With End-stage Joint Disease

A Phase 3 interventional study of oxycodone CR and oxycodone IR in Joint Diseases, Arthritis and Osteoarthritis, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.. Completed. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2012-02-13.

Sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C. · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
597
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The purpose of this study is to compare bowel function/constipation that occurs during tapentadol treatment with that occuring during oxycodone treatment, as measured by the frequency of spontaneous bowel movements per week. The frequency of spontaneous bowel movements will be determined from a Bowel Function Patient Diary completed by the enrolled sujbects.

Read the detailed description

Chronic pain from end-stage degenerative joint disease is often moderate to severe in intensity and results in a relatively constant level of pain requiring continuous pain relief medication. Despite available pain relief medications, 60% to 80% of subjects suffering from chronic pain are currently inadequately treated. Opioid pain medications are central to the effective treatment of moderate to severe pain. However, opioid therapy is frequently complicated by side effects. Constipation is one of the most commonly reported side effects and most debilitating. An opioid medication that provides pain relief with a reduced incidence of constipation symptoms would improve the capability of subjects to stay on medication to achieve the long-term relief they need. This is a randomized, double-blind, placebo- and active-controlled, parallel-arm, multicenter study with 4 treatment groups of subjects who have moderate to severe chronic pain from end-stage degenerative joint disease of the hip or knee and who are candidates for primary total or partial joint replacement. The study consists of 3 periods: a pretreatment period (a 14-day screening for study eligibility and a 7-day washout of any previously taken opioid medication), a double-blind treatment period (a 14-day IR treatment phase followed by a 28-day ER treatment phase), and a follow-up period (1 study-site visit within 4 days after the last dose of study drug is taken and 1 telephone contact within 10 to 14 days after the last dose of study drug is taken). On Day 1 of the IR treatment phase, patients will be randomly assigned to 1 of 4 possible treatment groups to receive 50 mg CG5503 IR, 75 mg CG5503 IR, 10 mg oxycodone IR, or placebo daily every 4 to 6 hours. At the beginning of the ER treatment phase, patients' study drugs will be transitioned to the ER form (by conversion from the IR to approximate equivalent total daily doses of the ER form) of their randomly assigned study drug of tapentadol ER, oxycodone CR, or placebo. The ER study drugs will be taken every 12 hours b.i.d. Dosages will be adjustable, with the study site personnel oversight, to ensure adequate pain relief is provided. Beginning with the washout period, patients will be given hand-held computer diaries in which to record their pain intensity, pain relief, bowel movement information, and answer questions on any nausea or vomiting that may occur. In addition, patients will write down the times and dosages of all medications they take during the study in a medication diary. Safety and tolerability will be assessed using physical examination, monitoring of adverse events, clinical and laboratory measures, and 12 lead ECG results. The first study hypothesis is that both tapentadol IR dosages are more effective than placebo in relieving pain based on the SPID score recorded by the patients over the first 5 days of the study. The second study hypothesis is that the Bowel Function Patient Diary results for both tapentadol IR dosages demonstrate improved tolerability compared to oxycodone IR 10 mg, based on the number of spontaneous bowel movements per week over the first 2 weeks of the study. In the IR treatment phase, each patient will take CG5503 IR 50 mg, CG5503 IR 75 mg, oxycodone IR 10 mg, or placebo orally every 4 to 6 hours for 14 days. In the ER treatment phase, dosages of the IR treatment groups will be converted to approximately equivalent dosages of the ER form of the assigned study drug: tapentadol ER, oxycodone CR, or placebo. Dosages may range from 100 to 500 mg/day of tapentadol ER and 20 to 60 mg/day of oxycodone CR taken orally 2x daily for 28 days.

02

Conditions studied

  • Joint Diseases
  • Arthritis
  • Osteoarthritis

Keywords

  • Pain medication
  • Arthritis
  • Joint pain
  • Analgesia
  • Analgesics
  • tapentadol
  • CG5503
  • Nucynta
03

In context

Arthritis

3,554 studies on the registry are indexed under Arthritis; 318 are open to participants now.

This study's enrollment of 597 is above the median of 90 across 2,377 interventional studies indexed under Arthritis.

Browse Arthritis studies →

Lead sponsor

Johnson & Johnson Pharmaceutical Research & Development, L.L.C. is the lead sponsor of 458 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • A clinical diagnosis of osteoarthritis of the hip or knee
  • End-stage degenerative joint disease
  • Eligibility for primary unilateral total or partial joint replacement surgery
  • Pain level moderate to severe and at such a level as to require daily doses of an opioid analgesic medication

Exclusion criteria

Exclusion Criteria:

  • Has a life-long history of seizure disorder or epilepsy
  • Had any of the following within the preceding 1 year: mild or moderate traumatic brain injury, stroke, transient ischemic attack, or brain neoplasm
  • Had a severe traumatic brain injury within 15 years of screening (consisting of one or more of the following: brain contusion, intracranial hematoma, either unconsciousness or post traumatic amnesia lasting for more than 24 hours)
  • Joint pain not associated with gout, fibromyalgia, rheumatoid arthritis, other autoimmune disease
  • History of alcohol or drug abuse
  • chronic hepatitis B and C or HIV, active hepatitis B and C within 3 months
  • Severely impaired renal function or moderately to severely impaired hepatic function
  • History of cancer within past 2 years
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
597 participants (actual)

Study arms

  • Experimental
    001

    Tapentadol IR (CG5503) 50mg for 14 days

    Drug: Tapentadol IR (CG5503)

  • Experimental
    002

    Tapentadol IR (CG5503) 75mg for 14 days

    Drug: Tapentadol IR (CG5503)

  • Active comparator
    003

    oxycodone IR 10mg for 14 days

    Drug: oxycodone IR

  • Placebo comparator
    004

    placebo 1 capsule for 14 days

    Drug: placebo

  • Experimental
    005

    Tapentadol ER (CG5503) flexible dose tablets and capsules 2 x a day for 28 days (100-500mg/day)

    Drug: Tapentadol ER (CG5503)

  • Active comparator
    006

    oxycodone CR flexible dose tablets and capsules 2 x a day for 28 days (20-60mg/day)

    Drug: oxycodone CR

  • Placebo comparator
    007

    placebo Tablets and capsules 2 x a day for 28 days

    Drug: placebo

Interventions

  • Drugoxycodone CR

    flexible dose tablets and capsules 2 x a day for 28 days (20-60mg/day)

  • Drugoxycodone IR

    10mg for 14 days

  • DrugTapentadol ER (CG5503)

    flexible dose tablets and capsules 2 x a day for 28 days (100-500mg/day)

  • DrugTapentadol IR (CG5503)

    50mg for 14 days

  • DrugTapentadol IR (CG5503)

    75mg for 14 days

  • Drugplacebo

    1 capsule for 14 days

  • Drugplacebo

    Tablets and capsules 2 x a day for 28 days

06

What researchers measure

Primary outcomes

  1. 5-Day Sum of Pain Intensity Difference (SPID5)

    SPID5 was calculated as the weighted (weights is taken as the number of hours elapsed since the previous measurement) sum of the PID collected up to 5 days. Pain intensity (PI) score is calculated as the average PI over the past 12 hours using an 11-point (0 to 10) numerical rating scale (NRS) where "0" is no pain and "10" is pain as bad as you can imagine. The difference between baseline PI at the qualifying period and current PI is pain intensity difference (PID).

    Time frame: Day 1 to Day 5

  2. Spontaneous Bowel Movements Per Week (SBMs/Week)

    The number of SBM over the 14-day IR treatment phase was determined from the Bowel Function Patient Diary and factored to enable a per week value to be used. An SBM is defined as any BM that has occurred without the use of a laxative, enema, suppository, or manual manipulation within the previous 24 hours.

    Time frame: Week 1 to Week 2

07

Results

Posted Feb 13, 2012

Participant flow

A total of 1000 participants were screened, 598 were randomized, 596 participants received medication in the first part of the double-blind treatment period (IR treatment phase). A total of 463 participants received medication in the second part of the double-blind treatment period (ER treatment phase).

IR Treatment
Participant flow — IR Treatment
MilestonePlaceboTapentadol 50 mgTapentadol 75 mgOxycodonePlacebo ERTapentadol EROxycodone CR
Started148151154143000
Completed132134126100000
Not completed16172843000
Withdrew: Adverse event481935000
Withdrew: Lack of efficacy4410000
Withdrew: Lost to follow-up1010000
Withdrew: Withdrawal by subject5146000
Withdrew: Resolution of pain0100000
Withdrew: Other2332000
ER Treatment
Participant flow — ER Treatment
MilestonePlaceboTapentadol 50 mgTapentadol 75 mgOxycodonePlacebo ERTapentadol EROxycodone CR
Started000012225091
Completed000011322676
Not completed000092415
Withdrew: Adverse event0000177
Withdrew: Lack of efficacy0000340
Withdrew: Lost to follow-up0000020
Withdrew: Withdrawal by subject0000253
Withdrew: Study medication non-compliant0000233
Withdrew: Other0000132

Outcome measures

Primary5-Day Sum of Pain Intensity Difference (SPID5)

SPID5 was calculated as the weighted (weights is taken as the number of hours elapsed since the previous measurement) sum of the PID collected up to 5 days. Pain intensity (PI) score is calculated as the average PI over the past 12 hours using an 11-point (0 to 10) numerical rating scale (NRS) where "0" is no pain and "10" is pain as bad as you can imagine. The difference between baseline PI at the qualifying period and current PI is pain intensity difference (PID).

Time frame:
Day 1 to Day 5
Reported as:
Mean · Units on a scale
5-Day Sum of Pain Intensity Difference (SPID5)
Units on a scalePlaceboTapentadol 50 mgTapentadol 75 mgOxycodone
5-Day Sum of Pain Intensity Difference (SPID5)98.6 ± 134.73153.1 ± 184.07161.8 ± 187.31218.4 ± 208.64
Statistical analysis
  • Placebo vs Tapentadol 50 mg · ANCOVA · p = 0.007 (P-value is adjusted for multiplicity for comparison against placebo using Hochberg's test.) · Difference in least-squares means: 55.1 · 95% CI 15.11 to 95.13The 95% confidence interval is unadjusted for multiplicity.
  • Placebo vs Tapentadol 75 mg · ANCOVA · p = 0.004 (P-value is adjusted for multiplicity for comparison against placebo using Hochberg's test.) · Difference in least-squares means: 63.4 · 95% CI 23.67 to 103.13The 95% confidence interval is unadjusted for multiplicity.
PrimarySpontaneous Bowel Movements Per Week (SBMs/Week)

The number of SBM over the 14-day IR treatment phase was determined from the Bowel Function Patient Diary and factored to enable a per week value to be used. An SBM is defined as any BM that has occurred without the use of a laxative, enema, suppository, or manual manipulation within the previous 24 hours.

Time frame:
Week 1 to Week 2
Reported as:
Mean · number of stools/week
Spontaneous Bowel Movements Per Week (SBMs/Week)
number of stools/weekPlaceboTapentadol 50 mgTapentadol 75 mgOxycodone
Spontaneous Bowel Movements Per Week (SBMs/Week)9.9 ± 5.169.0 ± 4.048.6 ± 4.656.7 ± 5.44
Statistical analysis
  • Placebo vs Oxycodone · ANCOVA · p = <0.001 (P-value is adjusted for multiplicity for comparison against Oxycodone using Hochberg's test.) · Difference in least-squares means: 3.1 · 95% CI 2.22 to 4.01The 95% confidence interval is unadjusted for multiplicity.
  • Tapentadol 50 mg vs Oxycodone · ANCOVA · p = <0.001 (P-value is adjusted for multiplicity for comparison against Oxycodone using Hochberg's test.) · Difference in least-squares means: 2.2 · 95% CI 1.34 to 3.12The 95% confidence interval is unadjusted for multiplicity.
  • Tapentadol 75 mg vs Oxycodone · ANCOVA · p = <0.001 (P-value is adjusted for multiplicity for comparison against Oxycodone using Hochberg's test.) · Difference in least-squares means: 1.6 · 95% CI 0.72 to 2.50The 95% confidence interval is unadjusted for multiplicity.

Adverse events

Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Placebo—1/148 (0.7%)48/148 (32.4%)
Tapentadol 50 mg—1/151 (0.7%)65/151 (43%)
Tapentadol 75 mg—0/154 (0%)88/154 (57.1%)
Oxycodone—1/143 (0.7%)98/143 (68.5%)
Placebo ER—0/122 (0%)23/122 (18.9%)
Tapentadol ER—1/250 (0.4%)80/250 (32%)
Oxycodone CR—0/91 (0%)36/91 (39.6%)
Most frequent serious events
Most frequent serious events
EventPlaceboTapentadol 50 mgTapentadol 75 mgOxycodonePlacebo ERTapentadol EROxycodone CR
Myocardial infarctionCardiac disorders0/1480/1510/1541/1430/1220/2500/91
Arteriosclerosis coronary arteryCardiac disorders1/1480/1510/1540/1430/1220/2500/91
Kidney infectionInfections and infestations0/1481/1510/1540/1430/1220/2500/91
Pulmonary embolismRespiratory, thoracic and mediastinal disorders0/1480/1510/1540/1430/1221/2500/91
Deep vein thrombosisVascular disorders0/1480/1510/1540/1430/1221/2500/91
Most frequent other events
Most frequent other events
EventPlaceboTapentadol 50 mgTapentadol 75 mgOxycodonePlacebo ERTapentadol EROxycodone CR
NauseaGastrointestinal disorders11/14826/15131/15457/1435/12223/25012/91
ConstipationGastrointestinal disorders22/14821/15128/15442/14310/12237/25018/91
VomitingGastrointestinal disorders1/1487/15113/15434/1435/12213/2506/91
DizzinessNervous system disorders6/14817/15135/15425/1434/1225/2503/91
SomnolenceNervous system disorders5/14820/15114/15417/1432/1228/2502/91
HeadacheNervous system disorders12/1486/1517/15415/1437/1228/2504/91
PruritusSkin and subcutaneous tissue disorders1/1482/1514/15413/1430/1223/2502/91
Dry mouthGastrointestinal disorders1/1484/1519/1546/1431/1223/2501/91
DiarrhoeaGastrointestinal disorders5/1484/1517/1545/1435/12213/2504/91

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)PlaceboTapentadol 50 mgTapentadol 75 mgOxycodoneTotal
<=18 years00000
Between 18 and 65 years110113114109446
>=65 years38384034150
Age Continuous
Age Continuous(years)PlaceboTapentadol 50 mgTapentadol 75 mgOxycodoneTotal
Mean58.8 ± 9.5758 ± 9.4758.4 ± 7.6659.4 ± 7.9458.7 ± 8.70
Sex: Female, Male
Sex: Female, Male(Participants)PlaceboTapentadol 50 mgTapentadol 75 mgOxycodoneTotal
Female100937581349
Male48587962247
Region Enroll
Region Enroll(Participants)PlaceboTapentadol 50 mgTapentadol 75 mgOxycodoneTotal
Canada32363734139
USA116115117109457
08

Study locations

No study locations are listed for this record.

09

References and documents

Publications

  • Etropolski M, Kelly K, Okamoto A, Rauschkolb C. Comparable efficacy and superior gastrointestinal tolerability (nausea, vomiting, constipation) of tapentadol compared with oxycodone hydrochloride. Adv Ther. 2011 May;28(5):401-17. doi: 10.1007/s12325-011-0018-0. Epub 2011 Apr 13. PubMed 21494892 ↗
10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 13, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT00784277
Lead sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Collaborators
Grünenthal GmbH
First posted
Nov 2, 2008
Start date
Oct 2008
Primary completion
Jul 2009
Completion
Jul 2009
Results posted
Feb 13, 2012
Last update
Feb 13, 2012

Study contacts

Johnson & Johnson Pharmaceutical Research & Development, L.L. C. Clinical Trial
study director · Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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