Achieving Target blood pressure goal in hypertensIon through hoME blood pressure monitoring during initiAl combInation therapy: A coMparative analysis - TIME AIM

Dr Nagaraj Desai0 个研究点目标入组 0 人开始时间: 待定最近更新: 2023年1月9日

试验速览

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•Patients meeting with following criteria to be included in the study:
•1. Male or female patients, age equal or >18 to equal or <85 years.
•2. Patients who have uncontrolled BP with monotherapy (SBP >140 & DBP >90 mmHg)
•3. Treatment naÃ¯ve patients diagnosed with stage 2 de novo hypertension as per ESC/ESH 2018 guidelines on hypertension management.
•4. Patients who are prescribed combination therapy as part of routine clinical practice by the study investigator.
•5. Patients willing to follow clinical study instructions and complete the patient diaries allotted to them.
•6. Patients or Legally acceptable representative of patient willing to provide written informed consent for participation in the clinical study.

•Patients meeting with following criteria to be excluded from the study:
•1. Female patients who are pregnant or breast feeding.
•2. Patients with known liver or kidney (patients who are diagnosed with stage 3 or more Chronic Kidney Disease) dysfunction.
•3. Patients who are consuming Ayurvedic/Herbal medicines which are intended for management of hypertension.
•4. Patients who are suspected of or known to have an intolerance to any of the drugs prescribed as combination therapy.
•5. Presence of any other clinically significant disease or laboratory findings that in the Investigators opinion may affect the study outcomes or continued participation of patient in the study.
•6. Participation in another study concurrently or within 4 weeks prior to the Screening Visit.

发起方

Dr Nagaraj Desai