COMPARISON OF AN EPHEDRINE CAFFEINE COMBINATION AND DEXFENFLURAMINE IN THE TREATMENT OF OBESITY - A DOUBLE-BLIND MULTICENTER TRIAL IN GENERAL-PRACTICE

被引:0
作者
BREUM, L
PEDERSEN, JK
AHLSTROM, F
FRIMODTMOLLER, J
机构
关键词
OBESITY; WEIGHT LOSS; CAFFEINE; EPHEDRINE; THERMOGENESIS; DEXFENFLURAMINE; APPETITE SUPPRESSANTS; GENERAL PRACTICE;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In previous separate studies, dexfenfluramine (DF) and ephedrine/caffeine (EC) have been shown to promote weight loss in obese patients as compared with placebo. In order to compare the efficacy and safety of these two anorectic drugs, 103 patients with 20-80% overweight were included in a 15-week double-blind study in general practice. Patients were randomized to either 15mg DF twice daily (n = 53), or 20 mg/200 mg ephedrine/caffeine three times a day (n = 50), supplementary to a 5 MJ/day diet. Forty-three patients from the DF group and 38 from the EC group completed the study. After 15 weeks of treatment, the DF group (n = 43) had lost 6.9 +/- 4.3 kg and the EC group (n = 38) had lost 8.3 +/- 5.2 kg (means +/- s.d., P = 0.12). In the subgroup of patients with BMI greater than or equal to 30 kg/m(2) (n = 59), the mean weight loss was 7.0 +/- 4.2 kg in the DF group (n = 29) and 9.0 +/- 5.3 kg in the EC group (n = 30), P < 0.05. Both systolic and diastolic blood pressures were reduced similarly during both treatments. Twenty-three patients in the DF group (43%) and 27 in the EC group (54%) complained of side-effects. Central nervous system side-effects, especially agitation, were more pronounced in the EC group (P < 0.05), whereas gastro-intestinal symptoms were more frequent in the DF group (P < 0.05). The side-effects declined markedly during the first month of treatment in both groups. In conclusion, DF and EC are comparable regarding efficacy and safety in the treatment of obesity in general practice. In patients with BMI greater than or equal to 30 kg/m(2), the EC treatment resulted in a slightly greater weight loss than DF treatment.
引用
收藏
页码:99 / 103
页数:5
相关论文
共 45 条
  • [31] Citalopram versus fluoxetine: A double-blind, controlled, multicentre, phase III trial in patients with unipolar major depression treated in general practice
    Patris, M
    Bouchard, JM
    Bougerol, T
    Charbonnier, JF
    Chevalier, JF
    Clerc, G
    Cyran, C
    VanAmerongen, P
    Lemming, O
    Petersen, HEH
    INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1996, 11 (02) : 129 - 136
  • [32] A double-blind, multicentre study to assess the tolerability and efficacy of paroxetine compared with amitriptyline in the treatment of depressed patients in Australian general practice
    Freed, E
    Goldney, R
    Lambert, T
    Tiller, J
    Johnston, R
    AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, 1999, 33 (03) : 416 - 421
  • [33] Reducing antibiotic use for uncomplicated urinary tract infection in general practice by treatment with uva-ursi (REGATTA) – a double-blind, randomized, controlled comparative effectiveness trial
    Kambiz Afshar
    Nina Fleischmann
    Guido Schmiemann
    Jutta Bleidorn
    Eva Hummers-Pradier
    Tim Friede
    Karl Wegscheider
    Michael Moore
    Ildikó Gágyor
    BMC Complementary and Alternative Medicine, 18
  • [34] Reducing antibiotic use for uncomplicated urinary tract infection in general practice by treatment with uva-ursi (REGATTA) - a double-blind, randomized, controlled comparative effectiveness trial
    Afshar, Kambiz
    Fleischmann, Nina
    Schmiemann, Guido
    Bleidorn, Jutta
    Hummers-Pradier, Eva
    Friede, Tim
    Wegscheider, Karl
    Moore, Michael
    Gagyor, Ildiko
    BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2018, 18
  • [35] The use of drug based on technologically processed antibodies to endocannabinoid receptor type 1 in the treatment of obesity in adults: results of a multicenter double blind placebo controlled randomized clinical trial
    Demidova, Tatiana Y.
    Krasil'nikova, Elena, I
    Vorob'ev, Sergey V.
    Morugova, Tatiana, V
    Adasheva, Tatiana, V
    TERAPEVTICHESKII ARKHIV, 2021, 93 (08) : 904 - 915
  • [36] Naltrexone plus bupropion combination medication maintenance treatment for binge-eating disorder following successful acute treatments: randomized double-blind placebo-controlled trial
    Grilo, Carlos M.
    Lydecker, Janet A.
    Gueorguieva, Ralitza
    PSYCHOLOGICAL MEDICINE, 2023, 53 (16) : 7775 - 7784
  • [37] Tolerability and efficacy of a combination of paracetamol and caffeine in the treatment of tension-type headache: a randomised, double-blind, double-dummy, cross-over study versus placebo and naproxen sodium
    Luigi Alberto Pini
    Enrico Del Bene
    Giorgio Zanchin
    Paola Sarchielli
    Girolamo Di Trapani
    Maria Pia Prudenzano
    Giovanni LaPegna
    Lidia Savi
    Giorgio Di Loreto
    Paolo Dionisio
    Franco Granella
    The Journal of Headache and Pain, 2008, 9 : 367 - 373
  • [38] Tolerability and efficacy of a combination of paracetamol and caffeine in the treatment of tension-type headache: a randomised, double-blind, double-dummy, cross-over study versus placebo and naproxen sodium
    Pini, Luigi Alberto
    Del Bene, Enrico
    Zanchin, Giorgio
    Sarchielli, Paola
    Di Trapani, Girolamo
    Prudenzano, Maria Pia
    LaPegna, Giovanni
    Savi, Lidia
    Di Loreto, Giorgio
    Dionisio, Paolo
    Granella, Franco
    JOURNAL OF HEADACHE AND PAIN, 2008, 9 (06) : 367 - 373
  • [39] Results of a multicenter, double-blind, randomized, parallel-group, placebo-controlled, single-dose study comparing the fixed combination of acetaminophen, acetylsalicylic acid, and caffeine with ibuprofen for acute treatment of patients with severe migraine
    Goldstein, Jerome
    Hagen, Martina
    Gold, Morris
    CEPHALALGIA, 2014, 34 (13) : 1070 - 1078
  • [40] Acetaminophen, aspirin, and caffeine in combination versus ibuprofen for acute migraine: Results from a multicenter, double-blind, randomized, parallel-group, single-dose, placebo-controlled study
    Goldstein, J
    Silberstein, SD
    Saper, JR
    Ryan, RE
    Lipton, RB
    HEADACHE, 2006, 46 (03): : 444 - 453