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Pharma standard (PS) supplements

Papers from the London sessions January 2018

First edition (2018)
BELCARO G., DUGALL M., LEDDA A.
A volume of 144 pages
Cover: paperback
ISBN-13 978-88-7711-940-7
Language: Italian

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Pharma-standard (PS) supplement registry studies define the field of activity of pharma-standard supplements and their possible, preventive, preclinical applications. The best fields of application for supplements are preclinical, borderline applications or the supplementary management of risk conditions. PS supplements studies procedure supplementary data to be compared to “background” historical data (i.e., based on the best available management for comparable subjects or conditions) or to other management plans. In these studies, the supplement or the combination of supplements was used according to the following rules:
1. The use of the supplement is suggested to the evaluation subjects; it is not prescribed but indicated as an option, possibly capable of improving the management of the risk condition;
2. The supplement is only used on top of what is considered the “standard” or best-management/care available, for that condition, according to international guidelines;
3. The use of the supplement should not interfere with any other treatment, management or preventive measure;
4. Time: the period of follow-up is considered variable, according to the needs and availability of the patients or registry subjects. The observation period - in these registries - is therefore variable, not prefixed. Ideally, the PS supplement should be used as long as needed to see results or changes:
5. The type of evaluation for these studies is always a registry.
The evaluation of the compliance concerning the use of the supplement is a significant value indicating how many subjects are willing to use the supplements. In these supplement studies sthere is no defined group allocation, no randomization organized by the investigators. Subjects decide - on the basis of an initial briefing - the management group they want to join including the control (non-supplement) group. No placebo is used. The evaluation of safety is absolutely essential. The field of PS supplements is expanding. Self-medication, individual management and “natural” products are more often considered with great attention. Most, high-quality products are available from the web from qualified sellers (i.e. Amazon). This meeting and this book present some interesting new research in the field of PS supplements and indicate new possible “soft” but effective management ways for many patients and physicians.
Contents
Behçet’s syndrome: effects of Pycnogenol® during regression phases
Clinical efficacy of Pycnogenol® supplementation in the remissive phases of Sjögren syndrome
Pycnogenol®: supplementary management of symptomatic osteoarthritis with a patch, an observational registry study
Pycnogenol® prevents oxidative stress and side effects in patients with hypothyroidism during levothyroxine treatment
Pycnogenol® supplementation improves the control of irritable bowel syndrome symptoms
Benign prostatic hyperthrophy: Pycnogenol® supplementation improves prostate symptoms and residual bladder volume
Temporary Kidney Dysfunction (TKD): Robuvit® supplementation in initial, transient kidney insufficiency and micro-macro albuminuria
Pycnogenol® supplementation in minimal cognitive dysfunction
Supplementation with Robuvit® in post-traumatic stress disorders associated to high oxidative stress
Improvement in mood, oxidative stress, fatigue and insomnia following supplementary management with Robuvit®
Centella Asiatica (Centellicum®) facilitates the regular healing of surgical scars in subjects at high risk of keloids
Mononucleosis-related fatigue. Supplementary management with Robuvit®
Prevention of symptoms associated to neck pain with a Pycnogenol® patch
Pycnogenol®: prevention of muscular mass and strength loss in the elderlies
Supplementation with Robuvit® in post-mastectomy-post radiation arm lymphedema

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