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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05561543
Other study ID # Peppermint oil hypertension
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 1, 2024
Est. completion date September 1, 2025

Study information

Verified date July 2023
Source University of Central Lancashire
Contact Jonathan Sinclair, DSc
Phone +447875651533
Email jksinclair@uclan.ac.uk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cardiovascular and associated hypertensive diseases are the leading health burden and cause of mortality worldwide; therefore, the necessity for effective interventions is paramount. Dietary interventions to improve cardiovascular health are highly sought after as they possess less risk and financial burden than pharmacological drugs. Our previous randomized trial has shown that oral peppermint can improving systolic blood pressure and other cardiovascular/ blood lipids in healthy individuals. However, to date, no research has explored this using a placebo randomized intervention in patients with hypertension. Therefore, the primary purpose of the proposed investigation is to test the ability of oral peppermint oil supplementation to improve cardiometabolic parameters in participants with mild-moderate hypertension.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date September 1, 2025
Est. primary completion date July 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: Meet 3 of 5 criteria for Metabolic Syndrome based on National Cholesterol Education Program-Adult Treatment Panel III guidelines: 1. Waist Circumference: >102cm (men), >88cm (women) 2. Fasting Triglycerides: =1.69 mmol.L-1 3. Fasting High Density Lipoprotein: <1.03 mmol.L-1 (men), <1.29 mmol.L-1 (women) 4. Blood Pressure: =130 mmHg SBP or =85 mmHg DBP 5. Fasting Glucose: =6.1 mmol.L-1 Exclusion Criteria: - Smoking current - Current or previous gastrointestinal, cardiovascular, hepatic or renal disease - Current diabetes or extreme hypertension (=160/100 mmHg) - Allergy to peppermint - Current medication (such as steroids, NSAIDs, antibiotics, antihypertensive, hypoglycaemic, lipid-lowering drugs) - Currently using any nutritional supplement. - Heavy alcohol consumption (>14 units per week).

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Peppermint oil
Peppermint oil
Other:
Placebo
Placebo

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Central Lancashire University of Hertfordshire

Outcome

Type Measure Description Time frame Safety issue
Primary Systolic blood pressure Systolic blood pressure - measured using a digital blood pressure monitor Baseline
Primary Systolic blood pressure Systolic blood pressure - measured using a digital blood pressure monitor 20 days
Secondary Diastolic blood pressure Diastolic blood pressure - measured using a digital blood pressure monitor Baseline
Secondary Diastolic blood pressure Diastolic blood pressure - measured using a digital blood pressure monitor 20 days
Secondary Percent bodyfat Participants percentage composition of fat - measured using bio-electrical impedance Baseline
Secondary Percent bodyfat Participants percentage composition of fat - measured using bio-electrical impedance 20 days
Secondary Waist circumference Waist circumference - measured using anthropocentric tape Baseline
Secondary Waist circumference Waist circumference - measured using anthropocentric tape 20 days
Secondary Waist to hip ratio Ratio of waist to hip circumference - measured using anthropocentric tape Baseline
Secondary Waist to hip ratio Ratio of waist to hip circumference - measured using anthropocentric tape 20 days
Secondary Resting metabolic rate Estimated daily calorie usage (Kcal) at rest - obtained using a metabolic cart through indirect calorimetry. Baseline
Secondary Resting metabolic rate Estimated daily calorie usage (Kcal) at rest - obtained using a metabolic cart through indirect calorimetry. 20 days
Secondary Resting utilization of carbohydrates Percent contribution of carbohydrate to daily calories - at rest - obtained using a metabolic cart through indirect calorimetry. Baseline
Secondary Resting utilization of carbohydrates Percent contribution of carbohydrate to daily calories - at rest - obtained using a metabolic cart through indirect calorimetry. 20 days
Secondary Resting utilization of fats Percent contribution of fats to daily calories - at rest - obtained using a metabolic cart through indirect calorimetry. Baseline
Secondary Resting utilization of fats Percent contribution of fats to daily calories - at rest - obtained using a metabolic cart through indirect calorimetry. 20 days
Secondary Blood glucose Capillary blood glucose - mmol/L Baseline
Secondary Blood glucose Capillary blood glucose - mmol/L 20 days
Secondary Blood triglycerides Capillary blood triglycerides - mmol/L Baseline
Secondary Blood triglycerides Capillary blood triglycerides - mmol/L 20 days
Secondary Blood cholesterol (Total, HDL & LDL) Capillary blood cholesterol - mmol/L Baseline
Secondary Blood cholesterol (Total, HDL & LDL) Capillary blood cholesterol - mmol/L 20 days
Secondary Capillary blood haemoglobin Capillary blood haemoglobin - g/L Baseline
Secondary Capillary blood haemoglobin Capillary blood haemoglobin - g/L 20 days
Secondary Triglyceride glucose index Log transformed measurement of the blood glucose and blood triglyceride measures outlined above. Baseline
Secondary Triglyceride glucose index Log transformed measurement of the blood glucose and blood triglyceride measures outlined above. 20 days
Secondary Coop-Wonka chart Psychological wellbeing - The Coop-Wonka chart is a six item questionnaire with a 1-5 scoring system for each thus the chart has a maximum score of 30 which indicates the lowest possible psychological Wellbeing. Baseline
Secondary Coop-Wonka chart Psychological wellbeing - The Coop-Wonka chart is a six item questionnaire with a 1-5 scoring system for each thus the chart has a maximum score of 30 which indicates the lowest possible psychological Wellbeing. 20 days
Secondary Beck Depression Inventory Psychological wellbeing - the Beck Depression Inventory is a 21 questionnaire with questions that range in scoring from 0-3, thus the maximum score is 63 which is the highest depression score possible. Baseline
Secondary Beck Depression Inventory Psychological wellbeing - the Beck Depression Inventory is a 21 questionnaire with questions that range in scoring from 0-3, thus the maximum score is 63 which is the highest depression score possible. 20 days
Secondary State Trait Anxiety Inventory Psychological wellbeing - the state trait anxiety inventory is a 40 item questionnaire with each question having a 1-4 score system, thus the maximum score is 80 which indicates the highest level of anxiety. Baseline
Secondary State Trait Anxiety Inventory Psychological wellbeing - the state trait anxiety inventory is a 40 item questionnaire with each question having a 1-4 score system, thus the maximum score is 80 which indicates the highest level of anxiety. 20 days
Secondary Insomnia Severity Index Sleep quality - The Insomnia Severity Index is a brief instrument designed to assess the severity of both nighttime and daytime components of insomnia. The Insomnia Severity Index is a 7-item self-report questionnaire yielding a total score ranging from 0 to 28. Baseline
Secondary Insomnia Severity Index Sleep quality - The Insomnia Severity Index is a brief instrument designed to assess the severity of both nighttime and daytime components of insomnia. The Insomnia Severity Index is a 7-item self-report questionnaire yielding a total score ranging from 0 to 28. 20 days
Secondary Pittsburgh Sleep Quality Index Sleep quality - The Pittsburgh Sleep Quality index, is a questionnaire that consists of 19 self-rated questions, grouped into 7 components. Each component is scored separately, weighted equally on a 0 - 3 scale and the scores of the 7 components are then added to give a global score, which has a range of 0 - 21 with higher scores indicating worse sleep quality. Baseline
Secondary Pittsburgh Sleep Quality Index Sleep quality - The Pittsburgh Sleep Quality index, is a questionnaire that consists of 19 self-rated questions, grouped into 7 components. Each component is scored separately, weighted equally on a 0 - 3 scale and the scores of the 7 components are then added to give a global score, which has a range of 0 - 21 with higher scores indicating worse sleep quality. 20 days
Secondary Epworth Sleepiness Scale Sleep quality - The Epworth Sleepiness Scale is a self-administered questionnaire with 8 questions. Respondents are asked to rate, on a 4-point scale (0-3) with a maximum score of 24. Baseline
Secondary Epworth Sleepiness Scale Sleep quality - The Epworth Sleepiness Scale is a self-administered questionnaire with 8 questions. Respondents are asked to rate, on a 4-point scale (0-3) with a maximum score of 24. 20 days
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