Phase 4
Completed N=1,059
An Efficacy and Safety Study of Tramadol Hydrochloride-Paracetamol in Treatment of Moderate to Severe Acute Neck-Shoulder Pain and Low Back Pain
Source: ClinicalTrials.gov NCT01843660 ↗Enrolled (actual)
1,059
Serious AEs
0.0%
Results posted
Aug 2013
Primary outcomePrimary: Pain Intensity Score Based on Numeric Rating Scale (NRS) at Hour 0.5 — 5.29 Units on a scale
Summary
The purpose of this study is to evaluate the efficacy and safety of tramadol hydrochloride-paracetamol tablets in treatment of moderate (medium level of seriousness) to severe (very serious) acute neck, shoulder and low back pain in orthopedics (pertaining to the bones) outpatient or emergency setting.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pain Intensity Score Based on Numeric Rating Scale (NRS) at Hour 0.5 |
5.29 | — |
| PRIMARY Pain Intensity Score Based on Numeric Rating Scale (NRS) at Hour 1 |
4.32 | — |
| PRIMARY Pain Intensity Score Based on Numeric Rating Scale (NRS) at Hour 2 |
3.52 | — |
| PRIMARY Pain Intensity Score Based on Numeric Rating Scale (NRS) at Hour 3 |
2.93 | — |
| PRIMARY Pain Intensity Score Based on Numeric Rating Scale (NRS) at Hour 4 |
2.56 | — |
| PRIMARY Pain Intensity Score Based on Numeric Rating Scale (NRS) at Hour 6 |
2.39 | — |
| PRIMARY Number of Participants With Pain Relief Score at Hour 0.5 |
7; 92; 209; 326; 394; 1 | — |
| PRIMARY Number of Participants With Pain Relief Score at Hour 1 |
46; 226; 271; 332; 154; 0 | — |
| PRIMARY Number of Participants With Pain Relief Score at Hour 2 |
104; 351; 270; 230; 74; 0 | — |
| PRIMARY Number of Participants With Pain Relief Score at Hour 3 |
179; 392; 307; 99; 52; 0 | — |
| PRIMARY Number of Participants With Pain Relief Score at Hour 4 |
222; 484; 194; 86; 43; 0 | — |
| PRIMARY Number of Participants With Pain Relief Score at Hour 6 |
304; 377; 218; 78; 51; 1 | — |
| SECONDARY Number of Participants Who Required Additional Dosage Administration |
97 | — |
| SECONDARY Number of Participants With Analgesic Satisfaction Score |
128; 659; 212; 29; 1 | — |
| SECONDARY Number of Participants With Overall Analgesic Satisfaction Score |
3; 39; 207; 669; 111; 1 | — |
Eligibility Criteria
Inclusion Criteria
- Intermittent or persistent pain for less than 3 months, required analgesic therapy, orthopedic surgery and emergency call participants suffering with severe neck, shoulder, low back pain or chronic neck, shoulder, lower back pain, acute (a quick and severe form of illness in its early stage) exacerbation pain
- Pain intensity to be assessed using Numerical Rating Scale (NRS), NRS score more than or equal to 4 (from 0 to 10, 0 = no pain, 10 = extreme pain)
- During normal pain and stable feeling, can study pain assessment methods and can fill in pain control diary
- Be willing to participate in the study and must give written informed consent
Exclusion Criteria
- Have used strong opium kind of medication 7 days prior to the enrolment
- Have severe mental disease or using antipsychotic (agent that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect) medication for medical treatment
- Drug abuse/dependence, or chronic alcohol abuse/depend on history
- Pregnant or lactating women
- Unable to tolerate tramadol or any failed treatment in past by using tramadol
- Comparatively more severe pain in other parts of the body than that of the pain mentioned in the research
Data sourced from ClinicalTrials.gov (NCT01843660). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.