CAPSACOX: Study Evaluating the Analgesic Efficacy of Capsaicin 8% Patches in Chronic Coccygodynia.
Study Details
Study Description
Brief Summary
The primary objective is to demonstrate the analgesic effect at day 60 of 8% capsaicin patch (Qutenza) for the treatment of patients with coccygodyinia.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 3 |
Detailed Description
This trial is a French, multicenter, randomized, controlled, bouble-blind and prospective study. Patients enrolled will be clinically followed for 5 months. The treatment duration per subject is 1 hour (1time).
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Capsaicin 179 mg cutaneous patch Capsaicin 179 mg cutaneous patch. 1 patch applied once for 1 hour at inclusion visit. |
Drug: Capsaicin 179 Mg Cutaneous Patch
1 patch applied once for 1 hour
Other Names:
|
| Placebo Comparator: Capsaicin low concentration patch Capsaicin 0.04 cutaneous patch. 1 patch applied once for 1 hour at inclusion visit |
Drug: Capsaicin low concentration patch (capsaicin 0,04%, 3,2 mg/cm2)
1 patch applied once for 1 hour
|
Outcome Measures
Primary Outcome Measures
- to demonstrate the analgesic effect at day 60 of 8% capsaicin patch (Qutenza) for the treatment of patients with coccygodyinia. [Day 60]
The difference in the proportion of subjects improved (PGIC≤2) in either treatment group at day 60. It is expected that there will be a difference of at least 20% between treatment arms.
Secondary Outcome Measures
- Evaluation of the tolerability of the 8% capsaicin patch compared to low concentration capsaicin patch (control) within the first 7 days [time 0 (prior to patch application), hour 1, 6, 12, 24, day 2 and day 7 and by collecting AEs during the study.time 0 (prior to patch application), hour 1, 6, 12, 24, day 2 and day 7 and through study completion (an average of 5 months)]
Tolerability will be assessed by the evolution over time of the pain intensity in standing position in the treated zone as measured on an 11 point numeric rating scale at time 0 (prior to patch application), hour 1, 6, 12, 24, day 2 and day 7 and by collecting AEs during the study.
- Evaluate the safety of the capsaicin 8% patch compared with the control patch throughout the study. [Throughout the study (an average of 5 months)]
Safety will be assessed by recording and describing adverse events throughout the study.
- Evaluation of the analgesic effect over time and maintenance of effect in the two treatment groups over the entire study. [Day 2, Day 7, Day 15, Day 21, Day 30, Day 45, Day 60, Day 90, Day 120 and Day 150.]
The timecourse of the analgesic effect will be measured by the Patients' Global Impression of Change (PGIC) scale and the area under the pain intensity score in sitting position as measured Day 2, Day 7, Day 15, Day 21, Day 30, Day 45, Day 60, Day 90, Day 120 and Day 150.
- Evaluation of health care consumption in the two treatment groups over the entire study period (5 months). [Over 5 months]
Care consumption will be assessed over 5 months using the Medication Quantification Scale (MQS), which provides a standardised assessment of consumption of analgesics and co-antalgesics.
- Evaluation of health care consumption in the two treatment groups over the entire study period (5 months). [Over 5 months]
Care consumption will be assessed over 5 months using a self-diary in which patients will enter the dates of medical consultations (psychiatry, rheumatology, general medicine, etc.), para-medical consultations and/or complementary medical consultations (physiotherapy, acupuncture, osteopathy, psychotherapy, etc.).
- Evaluation of the cost-utility of 8% capasaicin patch with common clinical practice over a time horizon of 5 months [Over a time horizon of 5 months]
The evaluation of cost-utility will be assessed as the ratio of the incremental cost-utility (RICU in cost per QALY gained) comparing the treatment with 8% capsaicin patch with usual practice according to the collective perspective and a 5-month horizon. QALYS will be calculated using patients' lifespan and a utility score obtained from responses to the EQ-5D-5L generic quality of life questionnaire.
- Analysis of primary and secondary endpoints according to the presence or absence of sacrococcygeal hypermobility. [At inclusion]
Subgroup analysis according to the presence or absence of a sacrococcygeal mobility disorder at inclusion for the primary endpoint and the first two secondary endpoints.
- Determination of the therapeutic response to 8% capsaicin patch [Day 60]
Measurement of the association between the patient's intrinsic clinical parameters and a therapeutic response to capsaicin defined by a PGIC ≤2.
- Sensitivity study to compare results on the primary endpoint by comparing data from the PGI-C and a comparison of the two numerical pain assessments at Day 0 and Day 60. [Between Day 0 and Day 60]
Comparison of the classification of patients as success-failure between PGI-C values at Day 60 (success if PGI-C≤2) and numerical pain assessments between Day 0 and Day 60 (success if there is a reduction of at least 2 points on the EN).
Eligibility Criteria
Criteria
Inclusion Criteria:
-
18 years old at the pre-inclusion visit
-
Presenting with chronic coccygodynia: pain in the coccygeal region, increased by sitting and or when rising from a sitting position and pain over the last ten days of intensity greater than or equal to four on the eleven-point numerical scale (from zero to ten) and having been present for more than 3 months.
-
Failure of previous treatments: NSAIDs, pressure-relieving cushions, infiltration (for hypermobile coccygodynia)
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Have never been treated with an 8% capsaicin patch for this indication
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With at least one clinical sign suggestive of neuropathic pain (burning, painful cold, numbness, tingling, electric discharge, allodynia of the gluteal groove, allodynia to pressure on the coccyx)
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Proficiency in reading and writing the French language
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Be affiliated to the social security system
-
Have signed an informed consent form
-
Women must meet one of the following criteria at the time of inclusion:
-
be using adequate contraceptive measures, and have a negative pregnancy test (specify if urine or blood test) prior to receiving the first dose of trial medication;
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or be post-menopausal (aged over 50 with amenorrhoea for at least 12 months after stopping all exogenous hormonal treatments)
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or (if under 50) have been in amenorrhoea for at least 12 months after stopping all exogenous hormone treatments and with luteinising hormone (LH) and follicle stimulating hormone (FSH) levels corresponding to post-menopausal levels.
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or have undergone irreversible surgical sterilisation by hysterectomy, bilateral oophorectomy or bilateral salpingectomy (this operation must be documented).
Exclusion Criteria:
-
Coccygodynia accompanied by a dermatological lesion in the intergluteal cleft (psoriasis, pilodinial cyste, wound)
-
Patients with other major pain disorders likely to interfere with pain assessment
-
Hypersensitivity to capsaicin or to one of the excipients
-
Adults under legal protection (guardianship, curatorship, legal protection)
-
Pregnant or breast-feeding women
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Brest University Hospital | Brest | France | ||
| 2 | Vendée Departmental Hospital | La Roche-sur-Yon | France | ||
| 3 | Confluent Private Hospital Centre | Nantes | France | ||
| 4 | Nantes University Hospital | Nantes | France | ||
| 5 | GH Paris saint Joseph | Paris | France | ||
| 6 | Rouen University Hospital | Rouen | France |
Sponsors and Collaborators
- Nantes University Hospital
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- RC22_0415