CTRI/2018/04/013439尚未招募4 期
A Prospective, Randomized, controlled, Parallel-group, and assessor-blind Clinical Trial of Comfort (P) gel Efficacy and Safety in the Management of Haemorrhoids.
GODS OWN STORE0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
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.Patients of either gender, aged >=18 years, with haemorrhoids (Grades 1, 2 or 3) confirmed by proctoscopy, visiting the OPD will be enrolled in the study.
- •2.Female subjects must have a negative pregnancy test. Pregnant patients will be excluded from the study.
- •3.Participants should be willing to sign a written consent for participation in the study and undergo a baseline interview.
- •4.Participants must be willing to commit to medication dosing and assessment visits for evaluation.
- •5.Participants must be willing to refrain from taking any other medications for treatment of haemorrhoids, including pain-killer, laxatives or stool softener, from the outset of the study until final evaluation (if patient force to take above said medicine, subject will be dropped from the study).
- •6.Participants must agree that during the study they will refrain from taking any new herbal supplement and prescription or non-prescription medications without prior approval of the research team.
- •7.Participants must agree to take healthy diet and life style.
排除标准
- •1.Patients with Grade 4/prolapsed haemorrhoids,
- •2. subjects who are pregnant or lactating mothers.
- •3.Patients currently using other anti-haemorrhoidal drugs or having taken any herbal medications in the last 30 days or planning to undergo any surgical procedure for haemorrhoids will be excluded from the study.
- •4.Patients with major hepatic, renal, or cardiovascular ailments will also be excluded from the study.
- •5.Participants with evidence or history of significant systemic, immunological, gastro-enteric or gastrointestinal disorder. (People with hypothyroidism who are on adequate and stable thyroid replacement will not be excluded).
- •6.Patients reporting use of laxative or stool softener during the study period.
- •7.Any participant who is not able to give adequate informed consent.
研究者
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