CTRI/2018/10/016051已完成4 期
A prospective, single-arm, open-label, multi-centric to determine the safety and effectiveness of Anafortan â??N. Fixed-dose combination of Camylofin Dihydrochloride 50mg and Nimesulide 100mg in patients with acute colicky abdominal pain in India - AHPLIN1701
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 295
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
- •Male or female patients aged >=18 years to 65 years
- •Patients presenting with acute colicky abdominal pain and having history of at least 1 episode within a 24 hour period prior to screening with no other concomitant illness.
- •Patients willing and able to provide written informed consent
排除标准
- •1.Patients with history of taking Anafortan-N® or any other prescription analgesics and antispasmodics medication (within the previous 1 weeks before study enrollment)
- •2.Pregnant and lactating women
- •3.History of hypersensitivity/allergy to study drug
- •4.Cognitive impairment, alcohol abuse, or psychiatric illness that would affect the ability of the patient to complete patient diary and other assessments
- •5.Any other illness or conditions that does not justify patientâ??s participation in the study as judged by the Investigator
- •6.Patients not willing to comply with the study procedures
研究者
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