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A Pilot Trial of Manlikang in Reducing Salt Intake and Blood Pressure Among Patients With Hypertension

Primary Purpose

Hypertension, Hypertension With Abnormal Renal Function

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
formula salt with very low sodium (Brand name: Manlikang)
Sponsored by
Peking University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypertension

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 50 to 75 years old
  • No planning to move out of the community in the next three months
  • Not cooking at home less than 3 times or one day during the study
  • Willing to participate in the study and sign informed consent

Exclusion Criteria:

  • Acute myocardial infarction, history of stroke in the past 3 months, history of malignancy or expected lifetime less than 1 year.
  • Hypercortisolism or aldosteronism
  • Acute disease, such as upper respiratory infection, fever and diarrhea.
  • Incapable of communicating, such as deaf and dumb, dementia, mental disorder.
  • Families taking salt substitute currently
  • Not willing to use Manlikang in family
  • Liver disfunction
  • Anyone with abnormal serum potassium in family
  • Anyone using potassium-retaining diuretics in family

Sites / Locations

  • Maoer Shi community

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

hypertension patients

Arm Description

Outcomes

Primary Outcome Measures

the change of systolic pressure
the change of systolic pressure before and after taking Manlikang

Secondary Outcome Measures

the change in 24-hour urine sodium
the change of 24-hour urine sodium before and after taking Manlikang
incidence of reducing antihypertensive drug dose
the incidence of reducing antihypertensive drug dose after taking Manlikang in each group.
incidence of reaching the normal blood pressure
blood pressure reaches the standard of systolic pressure<140mmHg and diastolic pressure<90mmHg after taking Manlikang.
adverse event
the adverse events after taking Manlikang

Full Information

First Posted
July 19, 2017
Last Updated
March 19, 2019
Sponsor
Peking University
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1. Study Identification

Unique Protocol Identification Number
NCT03226327
Brief Title
A Pilot Trial of Manlikang in Reducing Salt Intake and Blood Pressure Among Patients With Hypertension
Official Title
A Pilot Trial on Efficacy and Safety of a Formula Salt With Very Low Sodium (Manlikang) in Reducing Salt Intake and Blood Pressure Among Patients With Hypertension in Community
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
March 28, 2018 (Actual)
Primary Completion Date
July 30, 2018 (Actual)
Study Completion Date
July 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is a single arm trial with before-after comparison design. Three groups of patients with hypertension will be recruited: not taking antihypertension drugs and having normal renal function, taking antihypertension drugs and having normal renal function, and having abnormal renal function without regards of antihypertension drugs use. Each group includes 30 patients. Based on renal function test, the investigators provide the Manlikang containing potassium chloride to patients with normal renal function, and provide the Manlikang not containing potassium chloride to patients with abnormal renal function. All hypertension patients will use the formula salt with very low sodium (Manlikang) for six weeks, and will be followed up at 1, 2, 4 and 6 weeks. The primary outcome will be the decrease of patients' systolic blood pressure at the end of the trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Hypertension With Abnormal Renal Function

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
43 (Actual)

8. Arms, Groups, and Interventions

Arm Title
hypertension patients
Arm Type
Experimental
Intervention Type
Dietary Supplement
Intervention Name(s)
formula salt with very low sodium (Brand name: Manlikang)
Intervention Description
hypertension patients will use the formula salt with very low (<20%) sodium (Manlikang) for six weeks, and will be followed up at 1, 2, 4 and 6 weeks to assess the 24-hour urine sodium.
Primary Outcome Measure Information:
Title
the change of systolic pressure
Description
the change of systolic pressure before and after taking Manlikang
Time Frame
baseline and 6 weeks
Secondary Outcome Measure Information:
Title
the change in 24-hour urine sodium
Description
the change of 24-hour urine sodium before and after taking Manlikang
Time Frame
baseline and 6 weeks
Title
incidence of reducing antihypertensive drug dose
Description
the incidence of reducing antihypertensive drug dose after taking Manlikang in each group.
Time Frame
up to 6 weeks
Title
incidence of reaching the normal blood pressure
Description
blood pressure reaches the standard of systolic pressure<140mmHg and diastolic pressure<90mmHg after taking Manlikang.
Time Frame
up to 6 weeks
Title
adverse event
Description
the adverse events after taking Manlikang
Time Frame
up to 6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 50 to 75 years old No planning to move out of the community in the next three months Not cooking at home less than 3 times or one day during the study Willing to participate in the study and sign informed consent Exclusion Criteria: Acute myocardial infarction, history of stroke in the past 3 months, history of malignancy or expected lifetime less than 1 year. Hypercortisolism or aldosteronism Acute disease, such as upper respiratory infection, fever and diarrhea. Incapable of communicating, such as deaf and dumb, dementia, mental disorder. Families taking salt substitute currently Not willing to use Manlikang in family Liver disfunction Anyone with abnormal serum potassium in family Anyone using potassium-retaining diuretics in family
Facility Information:
Facility Name
Maoer Shi community
City
Chongqing
ZIP/Postal Code
400000
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
33441669
Citation
Liu T, Rao H, Wang M, Xu H, Wang W, Li G, Wang H, Mu L. Comparative analysis of visit and home blood pressure in a pilot trial on the effect of 18% sodium substitute salt on blood pressure. Sci Rep. 2021 Jan 13;11(1):907. doi: 10.1038/s41598-020-79282-2.
Results Reference
derived
PubMed Identifier
32080135
Citation
Mu L, Li C, Liu T, Xie W, Li G, Wang M, Wang R, Rao H, He Q, Wang W, Wu Y. A pilot study on efficacy and safety of a new salt substitute with very low sodium among hypertension patients on regular treatment. Medicine (Baltimore). 2020 Feb;99(8):e19263. doi: 10.1097/MD.0000000000019263.
Results Reference
derived

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A Pilot Trial of Manlikang in Reducing Salt Intake and Blood Pressure Among Patients With Hypertension

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