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OpenTrials
Completed

NCT Number: NCT06624423

Effect of Corn Silk Tea on Hypertension

Subjects having hypertension were divided into 3 groups. one control and two experimental who were provided with 2g and 4g of corn silk tea twice per day for 12 weeks.

Completed

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Key information

Age range

30 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institute of Food and Nutritional Sciences

Rawalpindi, Punjab Province, 50280, Pakistan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Subjects with Hypertension both male and female Subjects above age 30 years

-

Exclusion criteria

  • Subjects below age 30 years Pregnant and Lactating women Subjects with no co morbidities

Treatment and study plan

corn silk tea

Other

Corn Silk Tea

Primary outcomes

  1. Blood Pressure

    Time frame: 12 weeks

    Diastolic and Systolic blood pressure will be measured using a calibrated sphygmomanometer or an automatic digital blood pressure monitor.

    Measurements will be taken in a seated position after the participant will have rested for at least 5 minutes.

    Three readings will be taken at intervals of 1-2 minutes, and the average of these readings will be recorded to ensure accuracy.

Secondary outcomes

  1. Lipid Profile

    Time frame: 12 weeks

    Blood samples will be collected after an 8-12 hour overnight fast. Lipid profile will be measured using standard biochemical assays (such as enzymatic colorimetric methods) in a clinical laboratory. Total cholesterol, Low-Density Lipoproteins, High-Density Lipoproteins and Triglycerides were measured.

  2. Anthropometric Measurements

    Time frame: 12 weeks

    Body mass measurements and waist circumference will be measured. BMI will be calculated by measuring height and weight using a standard stadiometer and weighing scale,and applying the formula. BMI=weight in kg/height in m2 Waist circumference (WC) will be measured using a non-stretchable measuring tape, placed directly on the skin at the midpoint between the lower margin of the last palpable rib and the top of the iliac crest

Sponsors and collaborators

Lead sponsor

Pir Mehr Ali Shah Arid Agriculture University

Other

Registry information

Acronym: CST

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Oct 3, 2024
Registry last updated
Oct 3, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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