CTRI/2015/08/006090已完成3 期
A Randomized, Double Blind, Multicentric, Placebo Controlled, Parallel Group Clinical Trial To Evaluate the Efficacy and Safety of Prucalopride in Patients with Chronic Idiopathic Constipation
Torrent Pharamceutical Ltd0 个研究点目标入组 200 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Male or female patients having age 18 years to 65 years
- •2.Patient and/or his/her legally accepted representative willing to give written informed consent.
- •3.Patients with a diagnosis of chronic idiopathic constipation as per modified Rome II criteria.
- •Modified Rome II criteria: Patient reports fewer than three bowel movements (BMs) per week (with each BM occurring in the absence of any laxative, suppository, or enema use during the preceding 24 hr) and reports one or more of the following symptoms for at least 12 weeks, which need not be consecutive, in the 12 months before screening visit or before starting any chronic treatment for constipation.
- •very hard (little balls) and/or hard stools for at least 25% of the bowel movements
- •sensation of incomplete evacuation following at least 25% of the bowel movements
- •straining at least 25% of defecations
- •4.History of poor results with laxative treatment and diet counseling
- •5.Patients who report fewer than three complete spontaneous bowel movement (CSBMs) per week during pre-treatment period of 2 weeks after screening (verified at the time of enrolment visit).
排除标准
- •1.Patient with history of hypersensitivity to prucalopride or to any of the excipient.
- •2.Patients with mechanical bowel obstruction, megacolon/megarectum, or diagnosis of pseudo-obstruction (as per colonoscopy).
- •3.Patients with known or suspected organic disorders of the large or small bowel (e.g., inflammatory bowel disease, ulcerative colitis, Crohnâ??s Disease)
- •4. Patients with history of weight loss 10% of body weight over a period of 6 months.
- •5.Patients having history of anemia and Hb <=12.5 gm/dl for male or Hb <=12 gm/dl for female at screening laboratory investigation.
- •6.Patients on treatment with drugs which are likely to cause constipation e.g tricyclic antidepressants, anticholinergics, narcotic analgesics or calcium channel blockers.
- •7.Patients with active peptic ulcer.
- •8.Patient with history of bowel resection or rectal bleeding.
- •9.Patient with history of Hospitalization for any gastrointestinal or abdominal surgical procedure during the 3 months prior to screening.
- •10.Patients with TSH 6 µIU/ml or symptoms of hyperthyroidism or hypothyroidism and the same confirmed with laboratory investigation.
- •11.Patients with clinically significant ECG abnormalities or QTc 450 msec for male or QTc480 msec for female.
- •12.Clinically significant medical disorder or clinically significant abnormal laboratory finding.
- •13.History of faecal impaction that required hospitalization or have a history of laxative or enema abuse, ischemia colitis and pelvic floor dysfunction.
- •14.Patients with liver enzymes (ALT and AST) more than 2.5 times of the normal value and/or bilirubin more than 1.5 times of the normal value.
- •15.Patient with Serum creatinine more than upper limit of normal value (UNL).
- •16.Patient with history of malignancy except basal cell carcinoma
- •17.Pregnant or lactating women.
- •18.Female patients who are of childbearing potential and who are neither surgically sterilized nor willing to use reliable contraceptive methods (hormonal, barrier methods or intrauterine device)
- •19.Patient with history of alcohol or drug abuse in the opinion of the investigator.
- •20.Participation in any clinical study during last three months
研究者
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