Doxycycline for the Treatment of Nodding Syndrome
Ключевые слова
абстрактный
Описание
Primary hypothesis
Oral doxycycline 100mg daily for six weeks in patients with NS aged 8 years or older will reduce inflammatory responses and the proportion of patients with serum antibodies to NSPs or leiomodin 24 months after intervention by 40% compared to placebo.
Primary efficacy objective
To determine the effects of doxycycline 100mg daily for six weeks in patients with NS 8 years or older on serum levels of antibodies to NSPs (VGKC complex and others to be identified in a concurrent case-control study) or leiomodin at 24 months.
Study Type
This will be a two-arm, placebo-controlled (double blind) randomized phase II trial of oral doxycycline 100mg daily for six weeks.
Study site
Kitgum general hospital, Kitgum, Uganda.
Study Population
Study participants will be patients with confirmed NS as defined according to the World Health Organization (WHO) consensus case definition i.e. (i) Head nodding on two or more occasions, (ii) Occurring in clusters at a frequency of 5-20/minute, (iii) Onset between the ages of 3-18 years, (iv) Observed by a trained health worker or documented on EEG
Plus any one of:
a) triggered by food or cold weather; b) presence of other seizures or neurological abnormalities and cognitive decline and c) clustering in space or time), age ≥8 years, and with written consent from a parent or guardian.
Study Interventions
Participants will receive standard of care supportive treatment according to current guidelines for NS (antiepileptic drug treatment with sodium valproate, management of psychiatric disorders, nutritional, physical and occupational therapy as indicated).
All will be hospitalised in the first weeks during which period, baseline measurements including clinical assessments, EEG, cognitive and laboratory testing will be performed and antiepileptic drug doses rationalised.
Sample size: The sample size (115 participants per arm i.e. 230 total) is estimated based on the assumption that a six-weeks treatment course of doxycycline will reduce the proportion of participants with antibodies to NSPs or Leiomodin by 40% (from 50.0% to 30.0%) 24 months after initiation of the intervention while providing for 10% loss to follow-up (β=80%, α=0.05).
Participants will then be randomised to either oral doxycycline (Azudox®, Kampala Pharmaceutical Industries, Ltd) 100mg daily for six weeks or identical placebo. Treatment will be initiated in hospital but will be continued at home. Each participant will be visited at home at 2, 4 and 6 weeks for adherence monitoring and assessment of safety and will report back to the hospital study clinic at 6, 12 and 24 months.
Follow-up procedures:
Participants will be followed up at 2, 4, and 6 weeks by the health visitor to document adherence and assess safety and will be assessed for outcomes in hospital at 24 months after initiation of the intervention.
Data Analysis:
Primary analysis will be by intention to treat. The investigators will examine the effect of doxycycline at 24 months on antibodies to host NSPs and leiomodin, inflammatory responses (CRP, C3a and C3b), on epileptiform discharges and seizure control, and microfilaria density/ Wolbachia load, and on clinical (cognitive, motor, psychiatric and quality of life) symptoms compared to placebo.
In a sub-analysis, the investigators will examine the effects of the intervention in new patients compared to patients with long standing symptoms.
Даты
| Последняя проверка: | 01/31/2017 |
| Первый отправленный: | 03/08/2016 |
| Предполагаемая регистрация отправлена: | 07/26/2016 |
| Первое сообщение: | 07/31/2016 |
| Последнее обновление отправлено: | 02/21/2017 |
| Последнее обновление опубликовано: | 02/22/2017 |
| Фактическая дата начала исследования: | 09/04/2016 |
| Предполагаемая дата завершения начальной школы: | 04/04/2020 |
| Предполагаемая дата завершения исследования: | 08/04/2020 |
Состояние или болезнь
Вмешательство / лечение
Drug: Doxycycline
Other: Placebo
Фаза
Группы рук
| Рука | Вмешательство / лечение |
|---|---|
| Active Comparator: Doxycycline 115 participants will be randomized to oral Doxycycline 100 mg daily for six weeks.
Each capsule contains doxycycline hyclate equivalent to 100 mg of doxycycline base.
Treatment will be initiated in hospital but will be continued at home.
Scheduled study clinic and home visits will be conducted at 6, 12, 24 months and at 2, 4 and 6 weeks respectively for adherence monitoring and assessment of safety. | Drug: Doxycycline 115 participants will be randomized to either oral Doxycycline 100 mg daily for six weeks.
Treatment will be initiated in hospital but will be continued at home.
Scheduled study clinic visits will be made by the participants at 6, 12 and 24 months.
Each participant will be visited at home at 2, 4 and 6 weeks for adherence monitoring and assessment of safety |
| Placebo Comparator: Placebo 115 participants will be randomized to the placebo arm for matching capsules containing no active ingredients daily for six weeks.
Placebo will be initiated in hospital but will be continued at home.
Scheduled study clinic and home visits will be conducted at 6, 12, 24 months and at 2, 4 and 6 weeks respectively for adherence monitoring and assessment of safety. | Other: Placebo - Placebo (matching capsules containing no active ingredients) |
Критерии приемлемости
| Возраст, имеющий право на обучение | 8 Years Чтобы 8 Years |
| Полы, имеющие право на обучение | All |
| Принимает здоровых добровольцев | да |
| Критерии | Inclusion Criteria: 1. Participants with confirmed NS as defined by the WHO i.e. Head nodding on two or more occasions (both past and current) - Symptom onset between the ages of 3-18 years - Observed by a trained health worker or documented on EEG Plus any one of: - Triggered by food or cold weather - Presence of other seizures or neurological abnormalities and cognitive decline - Clustering in space or time. 2. Age 8 years or older 3. Written consent by the parent or guardian Exclusion Criteria: 1. Females with a positive urinary HCG (pregnancy) test 2. Patients receiving Phenobarbitone, Carbamazepine, Phenytoin or Rifampicin. 3. Known hypersensitivity to study drug 4. Withdrawal of consent since enrollment 5. Reported inability to swallow capsules 6. Enrolled or known agreement to enroll into another clinical trial involving ongoing or scheduled treatment with medicinal products during the course of the study 7. Suspected high likelihood of non-compliance with study drug and the follow-up schedule - e.g. dependent on a carer who is unlikely to consistently be available. |
Результат
Основные показатели результатов
1. Proportion of patients with antibodies to Neuron Surface Proteins (NSPs) or leiomodin at 24 months. [24 months]
Меры вторичного результата
1. Mean change in serum concentrations of antibodies to NSPs or leiomodin [From baseline (time 0 months) to 24 months]
2. Mean change in serum concentrations of C-Reactive Protein [From baseline (time 0 months) to 24 months]
3. Mean change in serum concentrations of C3a and C3b [From baseline (time 0 months) to 24 months]
4. Mean change in dermal microfilaria density on real time Polymerase Chain Reaction at 24 months [From baseline (time 0 months) to 24 months]
5. The proportions of patients achieving seizure freedom (≥1 month without head nodding or convulsive seizures) [24 months]
6. Proportion of patients with interictal epileptiform discharges on 30-minute diagnostic EEG [24 months]
7. Proportion of participants with Gross Motor Function Classification System (GMFCS) scores 3-5 [24 months]
8. Proportion of participants with mental health disorders on the Mini International Neuropsychiatric Interview for Children and Adolescents (MINI-KID) [24 months]
9. Mean change in cogstate scores [From baseline (time 0 months) to 24 months]
10. Proportion of participants with improved Quality of Life (a perception) on the Quality of Life in Childhood Epilepsy Questionnaire [From baseline (time 0 months) to 24 months]
11. Incidence rate of non-nodding syndrome sick clinic visits and all cause sick clinic visits [24 months]
12. The proportion of participants with stunting (height for age Z-scores <-3 SD) [24 months]
13. The proportion of participants with wasting (weight for height Z-scores <-3 SD) [24 months]
14. All-cause mortality [24 months]
15. Incidence rate of all-cause hospital admissions [24 months]
