Effectiveness of Bryophyllum in Nocturia-Therapy
Клучни зборови
Апстракт
Опис
In the therapeutic concept of the treatment of OAB, antimuscarinic drugs play a central role. Antimuscarinics are known to inhibit the contraction of detrusor muscle (smooth muscle cells) and block the muscarinic receptor (M2/M3) important for efferent nerve conduction. This conventional therapy for OAB can have important adverse effects, notably on the gastrointestinal tract with constipation, on the excretory glands in the sense of xerostomia/xerophthalmia, on the nerve cells of the brain inhibiting cognitive function and in the heart muscle cells accelerating the heart rate. Especially elderly people are affected by these undesirable effects. Because of changes in the receptor profile, the effect of antimuscarinics and improvement of symptoms might be lowered in elderly people and another substance with less side effects would be of great interest. No such adverse effects are reported for B. pinnatum. Until now, there are few data for its use in OAB. Efficacy and tolerability of B. pinnatum in the treatment of OAB are the major outcome measures of this clinical trial.
- 50 women are included in this observational study, treated with Bryophyllum pinnatum in form of the commercially available Bryophyllum tablets into capsules (verum: 2x2capsules/day). Recruitment time is planned from January, 2018 to January 2022.
- Duration of the drug administration is 3 weeks.
- Primary endpoint are the reduction of nocturia (measured by filling in a voiding dairy) and the change of sleep-quality (measured by using Pittsburgh Sleep Quality Index)
- secondary endpoints are the improvement of quality of life (measured by using the King's Health Questionnaire and the International Consultation on Incontinence Overactive Bladder Questionnaire (ICIQ-OAB), two questionnaires, validated for the German language and for women with incontinence), increase of the micturition volumes and reduction of urge episodes (measured by the patients and recorded in a voiding dairy) and the registration of adverse events during the study phase. Ethics committee approval has been given.
Датуми
Последен пат проверено: | 06/30/2020 |
Прво доставено: | 07/12/2020 |
Поднесено е проценето запишување: | 07/19/2020 |
Прво објавено: | 07/20/2020 |
Последното ажурирање е доставено: | 07/19/2020 |
Последно ажурирање објавено: | 07/20/2020 |
Крај на датумот на започнување на студијата: | 12/31/2017 |
Проценет датум на примарно завршување: | 01/05/2021 |
Проценет датум на завршување на студијата: | 08/11/2021 |
Состојба или болест
Интервенција / третман
Drug: Bryophyllum pinnatum
Фаза
Групи за раце
Рака | Интервенција / третман |
---|---|
Experimental: Bryophyllum pinnatum Bryophyllum pinnatum (BP) muscle relaxing substance | Drug: Bryophyllum pinnatum Bryophyllum is administered for 3 weeks. Bryophyllum is given in form of capsules, 350mg per capsule, 0-0-2-2/d: 2 capsules 30min. before supper,2 capsules before going to bed.
Other Names:
Bryophyllum pinnatum/Kalanchoe |
Критериуми за подобност
Возраст подобни за студии | 18 Years До 18 Years |
Полови квалификувани за студии | Female |
Прифаќа здрави волонтери | Да |
Критериуми | Inclusion Criteria: - Nocturia ≥2 Mal per a night - Overactive bladder (>8 Mictions/day) - Age > 18 Years - local or systemic Therapy with Estrogen, if the therapy dates >4 Weeks before study-start. - prior incontinence operation (if the operation dates back more than 6 months) - german speaking Patients and a given informed consent Exclusion Criteria: - Intolerance against a substance or a compound - participation in an other study 4 weeks prior to inclusion - urinary tract infection - drug abuse - bladder affecting drugs like anticholinergics, diuretics, muscle relaxing medicaments and phytotherapeutics - lactose intolerance - Pregnant and lactating women - Incompliance of Patient |
Исход
Мерки на примарниот исход
1. Reduction of nocturia frequency [4 Weeks]
2. Sleep-Quality. [4 Weeks]
Секундарни мерки на исходот
1. Changes of overactive bladder symptoms [before the second visit in 1 week, at follow-up control 3 weeks after begin of medication intake and 4 weeks after end of medication intake.]
2. Safety of Bryophyllum: adverse events [4 weeks]
3. Daytime sleepiness [before the second visit in 1 week, at follow-up control 3 weeks after begin of medication intake and 4 weeks after end of medication intake.]