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  1. Article ; Online: Kalium phosphoricum comp. in patients with neurasthenia: a randomized, double-blind, placebo-controlled clinical trial.

    Hellhammer, Juliane / Spitznagel-Schminke, Luitgard / Hufnagel, Rebecca

    Current medical research and opinion

    2024  Volume 40, Issue 2, Page(s) 239–251

    Abstract: Objective: This Phase IV placebo-controlled clinical trial was designed to demonstrate the efficacy and safety of the product Neurodoron (Kalium phosporicum comp., KPC) in patients with neurasthenia.: Methods: This monocenter, randomized, double- ... ...

    Abstract Objective: This Phase IV placebo-controlled clinical trial was designed to demonstrate the efficacy and safety of the product Neurodoron (Kalium phosporicum comp., KPC) in patients with neurasthenia.
    Methods: This monocenter, randomized, double-blind, placebo-controlled, parallel-group clinical trial (registration number: DRKS00003261) was conducted in an outpatient German trial site. Women and men aged 18 and above were randomized to receive either KPC or placebo if they reported typical symptoms of neurasthenia and a severe psychiatric disorder could be excluded. The primary objectives were a reduction in characteristic symptoms of nervous exhaustion and perceived stress as well as improvement in general health status after 6 weeks of treatment.
    Results: In total, 204 patients underwent screening, 78 were randomized in each treatment group, and 77 patients each received treatment (intention-to-treat (ITT) population = 154 patients). For none of the primary efficacy variables, an advantage in favor of KPC could be demonstrated in the pre-specified analysis (
    Conclusions: Trial treatment was well tolerated with only a few and minor AEs reported, confirming the markedly good safety of KPC. A significant improvement of neurasthenia was seen for the total study population at the end of the treatment period. Superiority of KPC vs. placebo could not be demonstrated with the pre-specified analysis with regards to a sum score of 12 typical symptoms, perceived stress, or general health status. However, the explorative post-hoc analysis revealed that KPC is superior to placebo in the characteristic symptoms irritability and nervousness. KPC could therefore be a beneficial treatment option for symptomatic relief of neurasthenia.
    MeSH term(s) Adult ; Female ; Humans ; Male ; Double-Blind Method ; Neurasthenia ; Treatment Outcome
    Language English
    Publishing date 2024-01-24
    Publishing country England
    Document type Clinical Trial, Phase IV ; Journal Article ; Randomized Controlled Trial
    ZDB-ID 80296-7
    ISSN 1473-4877 ; 0300-7995
    ISSN (online) 1473-4877
    ISSN 0300-7995
    DOI 10.1080/03007995.2023.2291169
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The Lubricating Effect of Eye Drops Containing Hyaluronic Acid and Mallow Extract in Patients with Dry Eye Disease-A Pilot Study.

    Basile, Andrea Attilio / Mandelli, Giulia / Cendali, Magda / Hufnagel, Rebecca

    Medicina (Kaunas, Lithuania)

    2023  Volume 59, Issue 5

    Abstract: Background and ... ...

    Abstract Background and Objectives
    MeSH term(s) Humans ; Hyaluronic Acid/adverse effects ; Ophthalmic Solutions/therapeutic use ; Pilot Projects ; Dry Eye Syndromes/drug therapy ; Dry Eye Syndromes/chemically induced ; Dry Eye Syndromes/diagnosis ; Italy ; Tears
    Chemical Substances Hyaluronic Acid (9004-61-9) ; Ophthalmic Solutions
    Language English
    Publishing date 2023-05-16
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2188113-3
    ISSN 1648-9144 ; 1010-660X
    ISSN (online) 1648-9144
    ISSN 1010-660X
    DOI 10.3390/medicina59050958
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Neurodoron® for Stress Impairments: A Prospective, Multicenter Non-Interventional Trial.

    Hellhammer, Juliane / Schmidt, Katja / Semaca, Cristina / Hufnagel, Rebecca

    Evidence-based complementary and alternative medicine : eCAM

    2022  Volume 2022, Page(s) 2626645

    Abstract: Introduction: Stress is associated with a multitude of physical and psychological health impairments. To tackle these health disorders, over-the-counter (OTC) products like Neurodoron® are popular since they are considered safe and tolerable. Experience ...

    Abstract Introduction: Stress is associated with a multitude of physical and psychological health impairments. To tackle these health disorders, over-the-counter (OTC) products like Neurodoron® are popular since they are considered safe and tolerable. Experience reports and first studies indicate that Neurodoron® is efficient in the treatment of stress-associated health symptoms. To confirm this, a non-interventional study (NIS) with pharmacies was conducted.
    Methods: The NIS was planned to enroll female and male patients who suffered from nervous exhaustion with symptoms caused by acute and/or chronic stress. The main outcome measures were characteristic stress symptoms, stress burden, and perceived stress. Further outcome measures included perceived efficacy and tolerability of the product as assessed by the patients and collection of adverse drug reactions (ADRs). A study duration of about 21 days with a recommended daily dose of 3-4 tablets was set.
    Results: 279 patients were enrolled at 74 German pharmacies. The analyzed set (AS) included 272 patients (mean age 44.8 ± 14.4 years, 73.9% female). 175 patients of the AS completed the NIS. During the study, all stress symptoms declined significantly (total score 18.1 vs. 12.1 (of max. 39 points),
    Language English
    Publishing date 2022-02-25
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2171158-6
    ISSN 1741-4288 ; 1741-427X
    ISSN (online) 1741-4288
    ISSN 1741-427X
    DOI 10.1155/2022/2626645
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Treatment of Functional Dyspepsia with a Fixed Peppermint Oil and Caraway Oil Combination Preparation as Compared to Cisapride

    Madisch, Ahmed / Heydenreich, Claus-Jürgen / Wieland, Veronika / Hufnagel, Rebecca / Hotz, Jürgen

    Arzneimittelforschung

    1999  Volume 49, Issue 11, Page(s) 925–932

    Abstract: The therapeutic equivalence of a fixed combination preparation consisting of peppermint oil and caraway oil (PCC, Enteroplant®) and the prokinetic agent cisapride (CIS, CAS 81098-60-4) was investigated in a four-week randomized controlled double-blind ... ...

    Abstract The therapeutic equivalence of a fixed combination preparation consisting of peppermint oil and caraway oil (PCC, Enteroplant®) and the prokinetic agent cisapride (CIS, CAS 81098-60-4) was investigated in a four-week randomized controlled double-blind study with planned adaptive interim analysis. The study comprised 120 outpatients with functional dyspepsia. The efficacy was evaluated in 118 patients. Of these, 60 patients received the enteric-coated combination preparation (2 × 1 capsule containing 90 mg peppermint oil + 50 mg caraway oil per day) and 58 patients received the reference preparation cisapride (3 × 10 mg/day). The mean reduction of the pain score (primary variable) recorded on a visual analog scale (VAS) during the four-week treatment was 4.62 points with the peppermint oil/caraway oil preparation. This score was comparable with the mean reduction under cisapride (4.60 points) (p = 0.021; test for equivalence). Equivalence was also found in the secondary variable “frequency of pain” with a reduction by 4.65 points under PCC and by 4.16 points under cisapride carried out on an exploratory basis (p = 0.0034). Comparable results were attained with both treatments in the Dyspeptic Discomfort Score which included the other dyspeptic symptoms as well as intestinal and extra- intestinal autonomic symptoms, in the prognosis as appraised by the physician and in the CGI scales (Clinical Global Impressions). Corresponding results were also found in Helicobacter pylori-positive patients and patients with initially intense epigastric pain in the two treat- ment groups. The combination preparation consisting of peppermint oil and caraway oil appears to be comparable with cisapride and provides an effective means for treatment of functional dyspep- sia. Both medications were tolerated well (adverse events were reported in 12 patients of the PCC group and in 14 patients of the CIS group).
    Keywords Caraway oil ; CAS 81098-60-4 ; Cisapride ; Dyspepsia ; functional ; Enteroplant®, clinical studies ; equivalence ; Peppermint oil
    Language German
    Publishing date 1999-11-01
    Publisher Editio Cantor Verlag
    Publishing place Stuttgart ; New York
    Document type Article
    ZDB-ID 502081-5
    ISSN 1616-7066 ; 0004-4172
    ISSN (online) 1616-7066
    ISSN 0004-4172
    DOI 10.1055/s-0031-1300528
    Database Thieme publisher's database

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