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临床试验/NCT03794388
NCT03794388已完成3 期

Multicentric, Open, Randomized Study Comparing Topical Treatment by Patch of Capsaicin to 8% (Qutenza) to Pregabalin Oral in the Early Treatment of Neuropathic Pain After Primary Surgery for Breast Cancer

Institut Cancerologie de l'Ouest22 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2019年3月19日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
140
试验地点
22
主要终点
To show the noninferiority of early early medical treatment by topical treatment with capsaicin compared to oral treatment of pregabalin on the evolution of neuropathic pain after 2 months in patients who have undergone surgical excision of breast cancer

研究概览

简要总结

Breast cancer is the most common cancer in women in Europe. Therefore, breast cancer has become a chronic disease and patients need to learn to live with it as well as with the adverse effects related to the disease itself or to the therapies used.

As noted in the third "Plan cancer", pain is a major criterion in the quality of life of patients treated for breast cancer.

Neuropathic pain was defined in 2011 by the international Association for the Study of Pain (I.A.S.P.) as the direct result of a lesion or disease affecting the somato-sensory system.

Surgical treatment is often the first treatment of breast cancer. It can be conservative by performing a partial mastectomy (lumpectomy or quadrantectomy) or non-preservative by total mastectomy.

Intercostobrachial neuralgia (NICB) or Post mastectomy painful Syndrome (MPRR) was first described by Wood in 1978 as "chronic pain beginning immediately or early after a mastectomy" Or a lumpectomy affecting the anterior thorax, armpit and/or arm in its upper half. These post-surgical pains are related to a lesion of the nerves in the breast area.

In particular, the intercostobrachial nerve can be severed, stretched or crushed during surgery.

Post-operative neuropathic pain in patients with breast cancer is underdiagnosed either by general practitioner or in a specialized environment.

The diagnosis of neuropathic pain is performed during examination and clinical examination. Several scales allow to detect neuropathic pain but only the DN4 is recognized to be the most specific and sensitive scale.

Patients do not always express this pain. They do not always reconcile with the surgery. Either because the pain occurs a long time after the surgery, or they find it normal to get hurt. These diagnostic difficulties cause a delay in setting up a suitable analgesic treatment.

However, neuropathic pain responds poorly to common analgesics. Diagnosis, evaluation and early management of neuropathic pain are a priority in order to avoid their chronicization, to improve the quality of life of patients with breast cancer and to enable them to return to work quickly.

We therefore assume that the diagnosis of early neuropathic pain at 2 months of surgery associated with initiation of appropriate topical treatment without the systemic effects of conventional oral treatments, would reduce the incidence of Chronic neuropathic pain 6 months after surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female who had first breast cancer surgery, regardless of the type of surgery
  • Age ≥ 18 years
  • Healthy, non-irritated skin on painful areas to treat
  • During the inclusion visit to M4 post surgery, neuropathic pain of the breast and / or axillary area corresponding to inter-brachial neuralgia with a DN4≥4 score.
  • Obtaining the signed written consent of the patient
  • Major patient affiliated to a social security scheme

排除标准

  • Contraindications specific to the treatments studied : capsaicine and pregabalin
  • Diabetic patient
  • Previous treatment with capsaicin or pregabalin
  • Opioid treatment> 80 mg / day (oral morphine equivalent) in progress- Topical treatment of pain between surgery and inclusion visit
  • Uncontrolled hypertension (systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 90 mmHg) or recent history (<3 months) of cardiovascular events (stroke, heart attack, pulmonary embolism)
  • Creatinine clearance (CLcr) <60mL / min according to the Cockcroft-Gault formula
  • Pregnant woman, likely to be pregnant or breastfeeding
  • Persons deprived of their liberty or guardianship (including curators),
  • Impossibility of submitting to the medical follow-up of the test for geographical, social or psychological reasons

研究组 & 干预措施

Arm CAPSAICINE topical

Experimental

Application of capsaicin patches at 8% on the painful area

1 to 2 patches will be administered during the consultation. If necessary, a second application will be realized 3 months later.

干预措施: Capsaicin (Drug)

Arm PREGABALINE

Active Comparator

Pregabalin tablets will be initiated at a dose of 50 mg / day taken in 2 doses Depending on the tolerance, the dose will be increased to 100 mg / day and then to 150 mg / day to reach a maximum dose of 600 mg / day.

An interval of 3 to 7 days must be observed between each dose increase.

干预措施: Pregabalin (Drug)

结局指标

主要结局

To show the noninferiority of early early medical treatment by topical treatment with capsaicin compared to oral treatment of pregabalin on the evolution of neuropathic pain after 2 months in patients who have undergone surgical excision of breast cancer

时间窗: 2 months

The 11-point numerical scale (0-10) is collected at 2 months.

次要结局

  • Regression of the painful area after 2 and 6 months of treatment between the two arms.(6 months)
  • Tolerance of each type of treatment by collecting side effects in each treatment arm.(6 months)
  • Impact of peri-surgical anxiety and depression on the development of neuropathic pain after surgery for breast cancer(49 months)
  • The evolution of the weight between the two arms after 6 months of treatment.(6 months)
  • To compare the efficacy of an early medical treatment with capsaicin topical treatment compared to oral treatment pregabalin on the evolution of neuropathic pain in patients who had undergone excision surgical breast cancer after 6 months of treatment(6 months)
  • To compare the functional change and quality of life perceived by patients after 2 and 6 months of treatment between the two arms: Questionnaire PGIC (patients' global impression of change)(6 months)
  • To compare the functional change and quality of life perceived by patients after 2 and 6 months of treatment between the two arms(6 months)
  • Proportion of patients for whom only 1 application has been sufficient.(6 months)
  • The incidence of NICBs 4 months after surgery for breast cancer(4 months)

研究者

发起方
Institut Cancerologie de l'Ouest
申办方类型
Other
责任方
Sponsor

研究点 (22)

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