Treatment of Neuropathic Pain in Leprosy

Pain, Neuropathic Clinical Trial

— AmyNeLe  

Official title:

Treatment of Neuropathic Pain in Leprosy: a Randomized Double Blind Controlled Study

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03324035
• Other study ID #: AmyNeLe
• Status: Active, not recruiting
• Phase: Phase 3
• Start date: March 1, 2017
• Est. completion date: August 1, 2022

Study information

• Verified date: February 2022
• Source: University of Sao Paulo
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Despite large efforts to eradicate leprosy, this curable mycobacterial infection still affects 250,000 new individuals annually. Half of the globe's leprosy patients live in Brazil and India. In 2013, 33,033 new leprosy cases diagnosed in Brazil, with an average incidence of 1.05 cases / 10 000 inhabitants. Recently a new concept of care after cure has called attention for severe pain in previously treated patients, particularly, neuropathic pain. Even so, until now no single drug has been studied for the treatment of pain in this patients, and the use of drugs is based on the study of other diseases. We designed the first placebo-controlled, double blinded randomized trial in the use of flexible-dose amitriptyline (tricyclic antidepressant) for the treatment of neuropathic pain related to leprosy

Description:

Despite large efforts to eradicate leprosy, this curable mycobacterial infection still affects 250,000 new individuals annually. Half of the globe's leprosy patients live in Brazil and India. In 2013, 33,033 new leprosy cases diagnosed in Brazil, with an average incidence of 1.05 cases / 10 000 inhabitants. Most new cases occur in economically restricted regions of the world, but because at least 5% of the general population is genetically susceptible to the causative agent, new cases may occur anywhere worldwide. This is especially true in times of high human geographic dislocation. Thus, leprosy should rank among the differential diagnosis list of general practitioners and specialists treating skin and peripheral nerve disorders even in non-endemic areas. Mycobacterium leprae is an obligatory intracellular bacterium that invades macrophages and Schwann cells. Although myelinating Schwann cells are relatively resistant to invasion, viable M. leprae cause marked myelin destruction and lead to secondary neuronal phenotypic changes, degeneration, and nerve dysfunction. Leprosy patients have historically been characterized by cutaneous insensibility in body areas of deformity, and the presence of pain in these patients has been neglected for a long time. It has only been recently acknowledged that leprosy can be associated with pain in general and neuropathic pain in particular. Leprosy patients frequently experience neuropathy in wide areas of the body, which may or may not present with pain. When pain exists, it may be acute or chronic, neuropathic or inflammatory. Leprosy has different clinical presentations (according to the host's innate immune response) that range from localized skin lesions and adjacent intra-epidermal nerve fiber injury to widespread neuropathy distributed in large areas of low body-surface temperature. Neuropathic pain in leprosy may affect 11-22% of patients, and up to 56% of those with chronic pain. Importantly, more than 85% of patients with leprosy-related neuropathic pain developed it after the end of the antimicrobial treatment period. This means that the majority of patients who developed neuropathic pain did so after they were formally cured of the disease, and, in many cases, discharged from medical assistance. Therefore, pain in leprosy can also be inserted as part of the "care after cure" program initiative, along with stigma, deformity and incapacity management strategies. In recent years several easy-to use screening tools have been developed to screen for neuropathic pain in leprosy patients, such as the douleur neuropathique-4 (DN-4) and others. These tools allow for the rapid (usually 20 seconds to administer) and reliable (high sensitivity) assessment of pain in leprosy patients. Additionally, very few reports have described he effects of treatment used for neuropathic pain in these patients, and no clinical trials have been conducted for this specific condition to date. One could argue that leprosy patients with neuropathic pain should respond to usual drugs such as tricyclic antidepressants and anticonvulsants (and they usually do), but the selection of the appropriate treatment regimen, the proper timing of treatment initiation and the most cost-effective drug is not an obvious task. Also, and very important, the lack of formal evidence-based data attesting the efficacy of tricyclics and anticonvulsants for the treatment of leprosy associated neuropathic pain hampers further a wider availability of these drugs in economically-restricted areas. All these limitations can be overcome if the current scientific interest in pain in leprosy is maintained and the present high-level research in the area continues to grow similarly to the previous decades. Here we designed the first placebo-controlled, double blinded randomized trial in the use of flexible-dose amitriptyline (tricyclic antidepressant) for the treatment of neuropathic pain related to leprosy. This study is currently approved by our local Ethics Review Board (CAAE: 45393415.9.0000.0068) and has stared the recruitment phase on March 2017. Recruitment time will be extended by 12 months due to dropouts related to the Covid pandemic. We have had dropouts due to a few patients developing covid and also due to patients having fear to become infected while attending hospital visits."

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 102
• Est. completion date: August 1, 2022
• Est. primary completion date: May 3, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

• Presence of spontaneous pain of medium intensity in the last 24 hours with a minimum value of 4 in 10 on a numerical scale, with a maximum of 10 points (summed pain questionnaire)
• Duration of pain of at least 6 months
• Presence of neuropathic pain "pure" or of clearly dominant character (no other pain, or pain associated unimportant)
• Pain due to leprosy confirmed by clinical examination and / or appropriate electrophysiological examination
• Ability to properly understand the Portuguese language, being able to understand the methodology of the study and questionnaires
• Having provided their consent in writing of their participation in the study

Exclusion Criteria:

• Linked to the disease in study:
• Neuropathic pain from other causes that not Hansen's disease (Diabetes, HIV, and after chemotherapy);
• Linked to the treatment:
• Hypersensitivity to amitriptyline and tramadol;
• Ongoing treatment with monoamine oxidase inhibitors (MAOIs);
• Cardiac and ophthalmologic disorders that contraindicate the use of amitryptiline;
• Pregnant or nursing women, or even women of childbearing age without the use of contraceptives.
• General
• Other pain with intensity higher then the neuropathic one;
• Ant other condition that may interfere with the evaluation of the study;
• Patients who have not given or signed the informed consent form;
• Incorrectly completion of the self-assessment of pain notebook in the period between inclusion and randomization (at least 4 scores in 7 days);
• Patients who can't be followed on a regular basis or that miss the appointments (we will give a 7 day tolerance for each appointment);
• Documented abuse of psychoactive drugs or alcohol;
• History of past or actual psychosis;
• Actual diagnosis of major depression following the DSM-IV criteria;
• Language and cognitive deficits that are capable of interfering with the understanding of the study;
• Patients not affiliated with a social security scheme (beneficiary or recipient);
• Patients who refuses to sign or are unable to understand the informed consent, under guardianship;
• Participation in other research protocol involving the use of any medication during the 30 days preceding the inclusion in the project.

Related Conditions & MeSH terms

• Amitriptyline
• Leprosy
• Leprosy Neuropathy
• Neuralgia
• Pain, Neuropathic

Intervention

Drug:
• Amitriptyline
Administer amitriptyline on flexible doses variating from 25mg to 75mg, with backup of tramadol, and evaluate the reduction of the pain based on the Brief Pain Inventory Questionnaire.
• Placebo oral capsule
Administer amitriptyline on flexible doses variating from 1 to 3 capsules, with backup of tramadol, and evaluate the reduction of the pain based on the Brief Pain Inventory Questionnaire.
• Tramadol
Administer to both arms on "as needed" scheme, to a maximum of 150mg/day.

Locations

Country	Name	City	State
Brazil	Hospital Das Clínicas da Faculdade de Medicina da USP	São Paulo	SP

Sponsors (2)

Lead Sponsor	Collaborator
University of Sao Paulo	Cristália Produtos Químicos Farmacêuticos Ltda.

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Reduction in pain intensity of 30% from baseline measured by verbal analog scale (VAS)	To evaluate the analgesic effect of amitriptyline in flexible dose in patients with neuropathic pain associated with leprosy compared to placebo on the Visual Analogic Scale (VAS) (range 100mm- minimum 0 and maximum 100)	63 days (9 weeks)
Secondary	Neuropathic pain	DN4 (douleur neuropathique 4) + (= 4/10)	63 days (9 weeks)
Secondary	Neuropathic Pain Symptoms	To assess the effectiveness of amitriptyline on the reduction of painful symptoms, and on neuropathic dimensions evaluated by the NPSI questionnaire (minimum 0 and maximum 100)	63 days (9 weeks)
Secondary	Mensure Quality of Life	To assess the impact of amitriptyline on the patient's quality of life, depressive and anxiety symptoms, quality of sleep, through the WHOQOL questionnaire (range 0 to 100).	63 days (9 weeks)
Secondary	Number of participants with treatment-related adverse events	To evaluate the number of participants with treatment-related adverse events as assessed by CTCAE v4.03 score 0/1 vs 2/3/4	63 days (9 weeks)
Secondary	Predictive factor of response	assess whether pain phenotype A (NPSI baseline score <15) responded differently to the active drug compared to phenotype B (NPSI score at baseline = 15)	63 days (9 weeks)
Secondary	Use of backup pain medication	To assess the difference in dosage of rescue medication (tramadol) between both treatment arms, by counting the number of pills of tramadol used by each patient.	63 days (9 weeks)