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Telmisartan 10 mg/amlodipine 1.25 mg/indapamide 0.625 mg for High Blood Pressure (GMRx2_PCT Trial)
Phase 3
Recruiting
Led By Anthony Rodgers, Professor
Research Sponsored by George Medicines PTY Limited
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 days
Treatment 3 months
Follow Up 1 months
Awards & highlights
GMRx2_PCT Trial Summary
This trial will test how well a combination of three low-dose drugs works to control blood pressure, compared to a placebo.
Eligible Conditions
- High Blood Pressure
GMRx2_PCT Trial Timeline
Screening ~ 3 days1 visit
Treatment ~ 3 months6 visits
Follow Up ~ 1 months1 visit
Screening ~ 3 days
Treatment ~ 3 months
Follow Up ~1 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Difference in change in home SBP from baseline to Week 4
Secondary outcome measures
Difference in change in clinic seated mean DBP from baseline to Week 4
Difference in change in clinic seated mean SBP from baseline to Week 4
Difference in change in home seated mean DBP from baseline to Week 4
+6 moreOther outcome measures
Safety Outcomes
GMRx2_PCT Trial Design
3Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: Triple ¼ (GMRx2)Experimental Treatment1 Intervention
Telmisartan 10 mg/amlodipine 1.25 mg/indapamide 0.625 mg
Group II: Triple ½ (GMRx2)Active Control1 Intervention
Telmisartan 20 mg/amlodipine 2.5 mg/indapamide 1.25 mg
Group III: PlaceboPlacebo Group1 Intervention
Placebo
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Logistics
Other reimbursement is provided
Other forms of reimbursement are provided for this trial.
Who is running the clinical trial?
George Medicines PTY LimitedLead Sponsor
2 Previous Clinical Trials
1,719 Total Patients Enrolled
Anthony Rodgers, ProfessorPrincipal InvestigatorThe George Institute
1 Previous Clinical Trials
1,385 Total Patients Enrolled
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