CTRI/2024/06/069356尚未招募2 期
A double-blind, randomized, placebo - controlled, pilot trial of individualized homoeopathic medicinesin Belching disorder in adults - nil
The Calcutta Homoeopathic Medical College and Hospital0 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
- 2 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 who will fulfill ROME IV diagnostic criteria for belching disorders:
- •a. Diagnostic Criteria for Belching Disorders Must include all the following: Bothersome
- •(severe enough to impact on usual activities) belching from the esophagus or stomach
- •more than 3 days a week.
- •b. Criteria fulfilled for the last 3 months with symptom onset at least 6 months before
- •2. Age between 18 and 65 years
- •3. Patients of either sex including transgender
- •4. Literate patients, ability to read English, Bengali or Hindi and illiterate people will be
- •interviewed by the investigators maintaining adequate privacy to fill up the scales or
- •questionnaires.
- •5. Willing to take part in the study and give written informed assent and/or consent voluntarily
排除标准
- •1. Patient of known case of any disease ofstomach or having any pathological condition causing
- •belching (e.g.: GERD, Peptic ulcer, Gastritis, Gastroparesis, Dumping syndrome etc.)
- •2. Patients having any other systemic disease or having any life-threatening illness affecting
- •quality of life or any other organ.
- •3. Necessary relevant diagnostic tests will be advised to exclude Patients having any
- •pathological conditions or organic diseases.
- •4. Patients who are taking any medicines regularly for these complaints within last 6 weeks.
- •5. Vulnerable population- Unconscious, ambulatory, too ill for consultation, differently abled,
- •terminally ill or critically ill patients, institutionalized persons, mentally disabled people.
- •6. Pregnant and postpartum women, nursing mothers.
- •7. Patients with the habit of tobacco chewing and/or smoking, alcoholism and/or any other
- •forms of substance abuse and/or dependence.
- •8. Self-reported immune-compromised condition.
- •9. Already been in homoeopathic treatment for any chronic illness for the last 6 months.
- •10. Simultaneous participation in any other clinical trial.
研究者
相似试验
进行中(未招募)
1 期
A randomized, double blind, placebo controlled, parallel-group, multi-centre, Phase IIb, study to determine the effect of BXL628 in women with detrusor overactivity - BXL628 effect in OABEUCTR2007-001214-16-GBBioXell SpA234
撤回
2 期
A randomized, double-blinded, placebo controlled, prospective, clinical phase II study to assess the safety and efficacy of expanded allogeneic adipose-derived stem cells (ASCs) for the treatment of complex perianal fistulas in Crohn???s disease.fistels10017969Crohn's DiseaseNL-OMON32259eids Universitair Medisch Centrum50
已完成
2 期
Study on finding the effect food supplement on indigestion or upper abdominal paiCTRI/2016/10/007386ITC LIFE SCIENCES AND TECHNOLOGY CENTER120
进行中(未招募)
不适用
A clinical trial in subjects who suffer from hay fever to see the effects of the study medication, SB-705498, when taken on its own or in conjunction with a background therapy, Fluticasone Propionate, on the symptoms triggered by an allergen challenge chamber session.EUCTR2011-000115-11-ATGlaxoSmithKline Research and Development Ltd72
已完成
不适用
To evaluate safety/tolerability and the efficacy of Supplement to improve function of liver in subjects with Non-Alcoholic Fatty Liver Disease (NAFLD).CTRI/2022/12/048588Sundyota Numandis Probioceuticals Pvt. Ltd.103
