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1.
Phytomedicine ; 18(8-9): 739-42, 2011 Jun 15.
Article in English | MEDLINE | ID: mdl-21514125

ABSTRACT

St. John's Wort (Hypericum perforatum L.) is a useful medication in the treatment of mild to moderate depression. By reanalysis of the data obtained from a total of 154 patients, who responded in a randomised, multicentric, double-blind, placebo-controlled study, to 6 weeks of treatment for an episode of moderate depression with either 20 mg citalopram or 900 mg Hypericum extract STW 3-VI, the duration of response and occurrence of relapse/recurrence were evaluated. Duration of response and occurrence of relapse/recurrence was measured by re-evaluating the responders in a controlled-clinical trial (final score of ≤10 according to HAMD at the end of the clinical trial) according to the Hamilton Rating Scale for Depression (HAMD). In total, 30 (19.5%) of the 154 responders were diagnosed with a relapse. The numbers of patients with relapses were highest in the citalopram group (14 of 54), whereas patients who were treated with Hypericum extract STW 3-VI showed the lowest relapse rate (8/54); patients from the placebo group showed a relapse rate of 8/46. No difference in the severity of relapse could be observed. The duration of response was longest for the Hypericum group (1817 days), intermediate for the citalopram group (1755 days) and shortest for the placebo group (802 days). Hypericum extract STW 3-VI is more efficient in lowering the relapse and recurrence rates of responders, when compared to citalopram and placebo. In addition, duration of response was increased in the group treated with Hypericum extract STW 3-VI.


Subject(s)
Citalopram/therapeutic use , Depressive Disorder/drug therapy , Hypericum/chemistry , Phytotherapy/methods , Plant Extracts/therapeutic use , Adolescent , Adult , Aged , Double-Blind Method , Female , Humans , Male , Middle Aged , Young Adult
3.
MMW Fortschr Med ; 146(Suppl 3-4): 99-106, 2004 Dec 09.
Article in German | MEDLINE | ID: mdl-15662899

ABSTRACT

Lecithin, a precursor of the neurotransmitter acetylcholine, has a positive effect on brain and memory functions. In a prospective, randomized, double-blind study, the effect of buerlecithin fluid (BLF) was investigated in comparison with placebo in patients with mild cognitive disorders. A total of 96 ambulatory patients (> 55 years) were admitted to the study. Treatment duration was 84 days. In both treatment groups, a clear improvement in all the cognitive parameters tested was seen. The main target measure, the overall Sandoz Clinical Assessment Geriatric (SCAG) score improved by 18.7 (test substance) and 16.4 (placebo) points (p = 0.1620). A statistically relevant improvement of the secondary target parameter, response in the SCAG score, was achieved with BLF (85.4%) in comparison with placebo (62.5%) (p = 0.018). Furthermore, BLF demonstrated significant superiority in a number of the other target measures. The study also confirmed the very good tolerability of BLF.


Subject(s)
Cognition Disorders/drug therapy , Phosphatidylcholines/therapeutic use , Aged , Cognition/drug effects , Cognition Disorders/diagnosis , Data Interpretation, Statistical , Double-Blind Method , Female , Geriatric Assessment , Humans , Male , Mental Status Schedule , Middle Aged , Phosphatidylcholines/administration & dosage , Phosphatidylcholines/pharmacology , Placebos , Prospective Studies , Psychiatric Status Rating Scales , Quality of Life , Time Factors , Treatment Outcome
4.
Cephalalgia ; 21(2): 120-8, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11422094

ABSTRACT

This study was a multinational, multicentre, double-blind, active controlled phase III trial designed to investigate efficacy and safety of 300 mg acetylsalicyclic acid (ASA) (n = 135) vs. 200 mg metoprolol (n = 135) in the prophylaxis of migraine. In total 270 (51 male and 219 female) patients, aged 18-65 years, suffering between two and six migraine attacks per month were recruited. The main objective was to show equivalence with respect to efficacy, defined as a 50% reduction in the rate of migraine attacks. A run-in phase was carried out with placebo for 4 weeks, followed by a 16-week drug phase. In both treatment groups the median frequency of migraine attacks improved during the study period, from three to two in the ASA group and from three to one in the metoprolol group; 45.2% of all metoprolol patients were responders compared with 29.6% with ASA. Medication-related adverse events were less frequent in the ASA group (37) than in the metoprolol group (73). The findings from this trial show that metoprolol is superior to ASA for migraine prophylaxis but has more side-effects. Acetylsalicylic acid is better tolerated than metoprolol. Using a strict responder criterion ASA showed a responder rate comparable with the placebo rate in the literature.


Subject(s)
Aspirin/administration & dosage , Metoprolol/administration & dosage , Migraine Disorders/drug therapy , Adolescent , Adult , Aged , Aspirin/adverse effects , Female , Humans , Male , Metoprolol/adverse effects , Middle Aged , Treatment Outcome
5.
Psychiatry Res ; 93(3): 209-16, 2000 Apr 10.
Article in English | MEDLINE | ID: mdl-10760379

ABSTRACT

In recent years it has been suggested that a serotonergic dysfunction is involved in the pathogenesis of obsessive-compulsive disorder (OCD). The loudness dependence of auditory evoked potentials (AEPs) is one of the best validated indicators of the activity of the serotonin system in humans. To explore the validity of the hypothesis of a serotonergic dysfunction in OCD, the loudness dependence of AEPs of 22 medication-free OCD patients were compared with those of 22 age- and gender-matched healthy subjects. Auditory evoked N1/P2 activity to tones of increasing intensity was studied using dipole source analysis. Contrary to the hypothesis, OCD patients and healthy controls did not differ in their LDAEPs of the tangential dipole in particular, located in the primary auditory cortex and closely related to central serotonergic activity. Furthermore, no significant correlation was found between the severity of obsessive-compulsive or depressive symptoms and the loudness dependence of AEPs. These findings do not support the hypothesis of a serotonergic dysfunction in OCD patients.


Subject(s)
Evoked Potentials, Auditory/physiology , Loudness Perception/physiology , Obsessive-Compulsive Disorder/physiopathology , Serotonin/physiology , Adult , Auditory Cortex/physiopathology , Brain Mapping , Female , Humans , Male , Middle Aged , Obsessive-Compulsive Disorder/diagnosis , Reference Values
6.
Unfallchirurgie ; 21(1): 50-3, 1995 Feb.
Article in German | MEDLINE | ID: mdl-7709496

ABSTRACT

Framycetin was tested against a variety of isolates of grampositive and gramnegative bacteria. The in-vitro activity of Framycetin against Staphylococcus aureus, Enterobacteriaceae, Pseudomonas aeruginosa as well as Pseudomonas fluorescens is today still favourable.


Subject(s)
Bacterial Infections/drug therapy , Cross Infection/drug therapy , Framycetin/therapeutic use , Bacterial Infections/microbiology , Cross Infection/microbiology , Dose-Response Relationship, Drug , Enterococcus/drug effects , Humans , Microbial Sensitivity Tests , Pseudomonas aeruginosa/drug effects , Staphylococcus/drug effects , Streptococcus/drug effects
7.
Lancet ; 340(8813): 254, 1992 Jul 25.
Article in English | MEDLINE | ID: mdl-1353188
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