CTRI/2012/01/002382已完成未知
A Multicentric Observational Pilot Study on Cost Analysis of ongoing Continuous Ambulatory Peritoneal Dialysis (CAPD) and Hemodialysis (HD) in India: Patient and Provider Perspectives
Baxter India Private Limited0 个研究点目标入组 80 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •1. Patients should be between 18-65 years of age
- •2.Patients should have completed minimum of 3 months on one mode of dialysis
- •3. Patients who are on HD for at least 10 sessions a month (prevalent practice)
- •4. Patients undergoing CAPD with at least 3 exchanges per day (prevalent practice)
- •5. Patients on dextrose based solutions for CAPD
- •6. Patients shifted from another renal replacement therapy but have completed 3 months on new modality
- •7. Patient willing to give informed consent
排除标准
- •1. Patients who are on dialysis for less than 3 months
- •2. Patients on Automated Peritoneal Dialysis
- •3. Patients using Extraneal as exchange fluid for PD
- •4. Patients with Hepatitis B & C and HIV infection
- •5. Patients having Charlson Co-morbidity index 5
- •6. Patients with mental or neurological disorders, that might make their survey questionable
- •7. Patients unwilling to cooperate
- •8. Patients with expected life expectancy less than 1 year
- •9. Pregnancy and women of child bearing age who are planning for conception in next 12 months (duration of the study)
- •10. Patients under any reimbursement or health insurance scheme without proper supporting bills
- •11. Patient expected to be transferred to a non participating center within the period of study
- •12. Patients who previously have received kidney transplant or intend to receive kidney transplant in next 3 months
- •13. Patients with concomitant participation in any other interventional study
研究者
相似试验
招募中
Unknown
A Prospective, Multi-Center, Pilot study to Evaluate the Efficacy and Safety of Fexuprazan based 7 days triple therapy for Eradication of Helicobacter pylori InfectionsKCT0008624Kyungpook National University Medical Center50
进行中(未招募)
1 期
A study to investigate the safety and tolerability of a 14 day oral treatment with different doses of BAY 1142524 in comparison to placebo in patients with left-ventricular dysfunction after myocardial infarction.EUCTR2014-005297-12-DKBayer HealthCare AG48
进行中(未招募)
1 期
A study to investigate the safety and tolerability of a 14 day oral treatment with different doses of BAY 1142524 in comparison to placebo in patients with left-ventricular dysfunction after myocardial infarction.EUCTR2014-005297-12-DEBayer AG48
已完成
不适用
A multicenter prospective observational study for the purpose of non-invasive diagnosis of post-transplant IgA nephropathy in the renal transplant recipientsJPRN-UMIN000021922Kagawa University Hospital200
尚未招募
不适用
A Multi-centre, Prospective Observational Study comparing Supervised Personal versus In-Lab Spirometry in Adults and Children with a Chronic Lung DiseaseACTRN12623000288628Royal Prince Alfred Hospital280
