Cuellar G E, Ruiz A M, Monsalve M C, Berber A
Módulo de diabetes del Hospital Psiquiátrico con Unidad de Medicina Familiar No. 10 Dr. Guillermo Dávilla García IMSS Delegación 04 del DF, Mexico City.
Obes Res. 2000 Jan;8(1):71-82. doi: 10.1038/oby.2000.10.
To evaluate the safety and efficacy of sibutramine 15 mg by mouth once per day in obese patients over a period of 6 months.
A monocenter, double-blind, placebo controlled, parallel, prospective clinical trial was carried out. Sixty-nine male and female obese patients (body mass index [BMI] > 30 kg/m2) aged 16 to 65 years entered the trial.
22 of 35 patients in the sibutramine group and 9 of 34 patients in the placebo group completed the trial. The high dropout rate in the sibutramine group was due to adverse events in 3 cases, lack of efficacy (as judged by patients) in 7, loss to follow-up in 2, and an orthopedic device being worn in 1; in the placebo group the dropouts were ascribed to lack of efficacy (as judged by patients) in 17 cases and to loss to follow-up in 8 cases. Using the method of last observation carried forward, the weight loss in the sibutramine group was 10.27 kg (95% confidence intervals [95% CI] 7.66; 13.07) and 1.26 kg (95% CI 0.3; 2.23) in the placebo group. The BMI loss was 4.17 kg/m2 (95% CI 3.11; 5.22) in the sibutramine group and 0.53 kg/m2 (95% CI 0.13; 0.92) in the placebo group. The waist circumference reduction was 12.51 cm (95% CI 9.25; 15.77) in the sibutramine group and 3.26 cm (95% CI 1.38; 5.14) in the control group (p<0.05 by paired Student's t test for all the intragroup comparisons). Twenty-three sibutramine patients had 34 adverse events, the most frequent adverse events in the sibutramine group were upper respiratory tract infections (n = 6) and constipation (n = 6); 16 placebo patients had 21 adverse events. Three sibutramine patients withdrew their informed consent when they had adverse events.
The results show that sibutramine induces significant loss of body weight and waist circumference. Cardiovascular function was not significantly affected by sibutramine. Sibutramine was well tolerated by most of the patients.
评估每日口服一次15毫克西布曲明,持续6个月对肥胖患者的安全性和有效性。
开展了一项单中心、双盲、安慰剂对照、平行、前瞻性临床试验。69名年龄在16至65岁之间的肥胖男性和女性患者(体重指数[BMI]>30kg/m²)进入试验。
西布曲明组35名患者中的22名以及安慰剂组34名患者中的9名完成了试验。西布曲明组的高退出率归因于3例不良事件、7例(由患者判断)缺乏疗效、2例失访以及1例佩戴矫形器械;在安慰剂组,退出者归因于17例(由患者判断)缺乏疗效和8例失访。采用末次观察结转法,西布曲明组体重减轻10.27千克(95%置信区间[95%CI]7.66;13.07),安慰剂组体重减轻1.26千克(95%CI0.3;2.23)。西布曲明组BMI降低4.17kg/m²(95%CI3.11;5.22),安慰剂组降低0.53kg/m²(95%CI0.13;0.92)。西布曲明组腰围减少12.51厘米(95%CI9.25;15.77),对照组腰围减少3.26厘米(95%CI1.38;5.14)(所有组内比较经配对t检验,p<0.05)。23名服用西布曲明的患者出现34次不良事件,西布曲明组最常见的不良事件是上呼吸道感染(n=6)和便秘(n=6);16名服用安慰剂的患者出现21次不良事件。3名服用西布曲明的患者在出现不良事件时撤回了知情同意书。
结果表明,西布曲明可显著减轻体重和减小腰围。西布曲明对心血管功能无显著影响。大多数患者对西布曲明耐受性良好。