跳至主要内容
临床试验/NCT02435693
NCT02435693已完成不适用

Evaluation of Pharmaceutical Care Program for Type 2 Diabetes Mellitus in Dhule

TABREJ MUJAWAR2 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2012年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
600
试验地点
2
主要终点
Fasting blood glucose measurements recorded (mg/dl).Postprandial blood glucose Recorded: Fasting blood glucose measurements recorded (mg/dl).Postprandial bloodglucoseRecorded

研究概览

简要总结

Evaluation of Pharmaceutical Care Program for Type 2 diabetes mellitus in Dhule

Objectives:-

  1. To evaluate Pharmaceutical care program in Type2 diabetics.
  2. To evaluate the impacts of Pharmaceutical care on quality of life (QOL) in patient with Type-2 Diabetes Mellitus.
  3. To study the prevalence of Type2 diabetics cases in Dhule.
  4. To study the Assessment of different type of adverse drug reactions (ADRs). In Type2 diabetics.
  5. To evaluate the Drug Drug intereaction in Type-2 Diabetes Mellitus.
  6. To study the impacts of Pharmaceutical care program on glycemic control in patients with Type-2 Diabetes Mellitus.
  7. To study the Drug utilization pattern in Type-2 Diabetes Mellitus in civil hospital Dhule.
  8. To compare the efficiency of Pharmaceutical care program and drug in patients with Type-2 Diabetes Mellitus.
  9. To study the Pharmaco-economic evaluation in Type-2 Diabetes Mellitus patient's.
  10. To increase the patient compliance and positive attitude of patients towards the diabetes disease by counseling.

详细描述

To evaluate the impacts of Pharmaceutical care on quality of life (QOL) in patient with Type-2 Diabetes Mellitus.

To study the prevalence of Type2 diabetics cases in Dhule. To study the Assessment of different type of adverse drug reactions (ADRs). In Type2 diabetics.

To evaluate the Drug Drug intereaction in Type-2 Diabetes Mellitus.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
35 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Inclusion Criteria:
  • Patients with type 2 diabetes mellitus of either
  • Patients with HbA1c more than 7% and
  • Patients with blood sugar level more than 140 mg / dl

排除标准

  • Patient with end stage kidney disease.
  • Patient with heart failure.
  • Patient with chronic Diabetes problem and orthopedic problem

结局指标

主要结局

Fasting blood glucose measurements recorded (mg/dl).Postprandial blood glucose Recorded: Fasting blood glucose measurements recorded (mg/dl).Postprandial bloodglucoseRecorded

时间窗: 24 weeks

Fasting blood glucose measurements recorded (mg/dl).Postprandial blood glucose Recorded Fasting blood glucose measurements recorded (mg/dl).Postprandial blood glucose Recorded fasting blood glucose

次要结局

  • Quality of Life score(24 weeks)

研究者

发起方
TABREJ MUJAWAR
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

TABREJ MUJAWAR

tabrej mujawar mpharm Study principal investigator

R. C. Patel Institute of Pharmaceutical Education & Research

研究点 (2)

Loading locations...

相似试验