An Asia-Pacific, double blind, placebo controlled, randomised study to evaluate the efficacy, safety, and tolerability of tegaserod in patients with irritable bowel syndrome

被引:168
作者
Kellow, J
Lee, OY
Chang, FY
Thongsawat, S
Mazlam, MZ
Yuen, H
Gwee, KA
Bak, YT
Jones, J
Wagner, A
机构
[1] Novartis Pharma AG, CH-4056 Basel, Switzerland
[2] Royal N Shore Hosp, Sydney, NSW, Australia
[3] Hanyang Univ, Med Ctr, Seoul 133791, South Korea
[4] Vet Gen Hosp, Taipei, Taiwan
[5] Chiang Mai Univ Hosp, Chiang Mai, Thailand
[6] Princess Margaret Hosp, Kuala Lumpur, Malaysia
[7] Natl Univ Singapore Hosp, Singapore, Singapore
[8] Korea Univ, Med Ctr, Seoul 136701, South Korea
[9] Ampnag Puteri Specialist Hosp, Kuala Lumpur, Malaysia
关键词
D O I
10.1136/gut.52.5.671
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Tegaserod has been shown to be an effective therapy for the multiple symptoms of irritable bowel syndrome (IBS) in Western populations. However, little information is available regarding the use of tegaserod in the Asia-Pacific population. Aims: To evaluate the efficacy, safety, and tolerability of tegaserod versus placebo in patients with IBS from the Asia-Pacific region. Patients: A total of 520 patients from the Asia-Pacific region with IBS, excluding those with diarrhoea predominant IBS. Methods: Patients were randomised to receive either tegaserod 6 mg twice daily (n=259) or placebo (n=261) for a 12 week treatment period. The primary efficacy variable (over weeks 1-4) was the response to the question: "Over the past week do you consider that you have had satisfactory relief from your IBS symptoms?" Secondary efficacy variables assessed overall satisfactory relief over 12 weeks and individual symptoms of IBS. Results: The mean proportion of patients with overall satisfactory relief was greater in the tegaserod group than in the placebo group over weeks 1-4 (56% v 35%, respectively; p<0.0001) and weeks 1-12 (62% v 44%, respectively; p<0.0001). A clinically relevant effect was observed as early as week 1 and was maintained throughout the treatment period. Reductions in the number of days with at least moderate abdominal pain/discomfort, bloating, no bowel movements, and hard/lumpy stools were greater in the tegaserod group compared with the placebo group. Headache was the most commonly reported adverse event (12.0% tegaserod v 11.1% placebo). Diarrhoea led to discontinuation in 2.3% of tegaserod patients. Serious adverse events were infrequent (1.5% tegaserod v 3.4% placebo). Conclusions: Tegaserod 6 mg twice daily is an effective, safe, and well tolerated treatment for patients in the Asia-Pacific region suffering from IBS and whose main bowel symptom is not diarrhoea.
引用
收藏
页码:671 / 676
页数:6
相关论文
共 32 条
  • [1] CHATELLIER G, 1966, BMJ-BRIT MED J, V312, P426
  • [2] Antinociceptive properties of HTF 919 (tegaserod), a 5-HT4 receptor partial agonist, on colorectal distension in rats.
    Coelho, AM
    Rovira, P
    Fioramonti, J
    Bueno, L
    [J]. GASTROENTEROLOGY, 2000, 118 (04) : A835 - A835
  • [3] Coffin B, 2002, GASTROENTEROLOGY, V122, pA311
  • [4] Tegaserod, a 5-HT4 receptor partial agonist, accelerates gastric emptying and gastrointestinal transit in healthy male subjects
    Degen, L
    Matzinger, D
    Merz, M
    Appel-Dingemanse, S
    Osborne, S
    Lüchinger, S
    Bertold, R
    Maecke, H
    Beglinger, C
    [J]. ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2001, 15 (11) : 1745 - 1751
  • [5] Irritable bowel syndrome: A technical review for practice guideline development
    Drossman, DA
    Whitehead, WE
    Camilleri, M
    [J]. GASTROENTEROLOGY, 1997, 112 (06) : 2120 - 2137
  • [6] Drossman DA, 2000, ROME 2 FUNCTIONAL GA, P360
  • [7] Drossman Douglas A., 1999, American Journal of Medicine, V107, p41S
  • [8] *EUR AG EV MED PRO, 2002, POINTS CONS EV MED P
  • [9] Fidelholtz J, 2002, AM J GASTROENTEROL, V97, P1176
  • [10] Gershon MD, 1999, ALIMENT PHARM THER, V13, P15