Potassium-Magnesium Citrate as a Blood Pressure Lowering Agent in Hypertensive Patients
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ClinicalTrials.gov Identifier: NCT01074918 |
Recruitment Status :
Withdrawn
(none enrolled per PI)
First Posted : February 24, 2010
Last Update Posted : February 11, 2019
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Pre-hypertension Hypertension | Drug: Potassium, Magnesium, Citrate Drug: Potassium Chloride | Phase 1 Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 0 participants |
Allocation: | Randomized |
Intervention Model: | Crossover Assignment |
Masking: | Triple (Participant, Care Provider, Investigator) |
Primary Purpose: | Supportive Care |
Official Title: | Potassium-Magnesium Citrate as a Blood Pressure Lowering Agent in Hypertensive Patients; Role of Natriuresis |
Study Start Date : | September 2009 |
Actual Primary Completion Date : | September 2012 |
Actual Study Completion Date : | December 2012 |

Arm | Intervention/treatment |
---|---|
Experimental: Potassium Magnesium Citrate |
Drug: Potassium, Magnesium, Citrate
Potassium MAgnesium Citrate - 30 mEq potassium, 15 mEq Magnesium, 45 mEq Citrate in a powder mixture twice a day, mixed with a glass of water. |
Active Comparator: Potassium Chloride |
Drug: Potassium Chloride
Potassium Chloride |
- Blood Pressure [ Time Frame: 8 weeks ]We have estimated to detect a 4 mmHg difference, with a standard deviation estimated at 8 mmHg.

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Ages Eligible for Study: | 21 Years to 95 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Age greater than 21 years
- BMI > 18.5 kg/m2 and < 40 kg/m2
- Prehypertension and mild hypertension: BP systolic 120-159 mmHg, diastolic 80-95 mmHg
- Must agree to limit lifestyle changes including: 1) embarking on a new exercise or weight reduction program 2) altering alcohol intake during the trial.
Exclusion Criteria:
- Taking blood pressure lowering medication
- Diabetes mellitus
- Renal disease
- Active cardiac disease
- Active liver disease
- Chronic diarrhea
- Chronic NSAID use
- Active or suspected drug use
- Uncontrolled psychiatric disease
- HIV infection
- Missed more than 20% of clinic visits in the last yr
- Prescription of diuretics for any reason
- A patient taking nutritional supplements including multivitamins that is unwilling to discontinue them,\
- Consumption of greater than 14 alcoholic beverages per week

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01074918
United States, Texas | |
Dallas VA Medical Center | |
Dallas, Texas, United States, 75216 | |
UT Southwestern Medical Center | |
Dallas, Texas, United States, 75390 |
Responsible Party: | Orson Moe, Professor of Internal Medicine, University of Texas Southwestern Medical Center |
ClinicalTrials.gov Identifier: | NCT01074918 |
Other Study ID Numbers: |
012007-080 |
First Posted: | February 24, 2010 Key Record Dates |
Last Update Posted: | February 11, 2019 |
Last Verified: | February 2019 |
Pre-hypertension Hypertension |
Hypertension Prehypertension Vascular Diseases Cardiovascular Diseases |