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Evaluating the effectiveness of Rosa canina L. fruit syrup on hypertension, cholesterol and anxiety In patients with hypertension

Evaluating the effectiveness of Rosa canina L. fruit syrup on hypertension, cholesterol and anxiety In patients with hypertension A double-blind randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211017052785N1
Enrollment
80
Registered
2022-03-26
Start date
2022-07-06
Completion date
Unknown
Last updated
2022-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HTN. Essential (primary) hypertension

Interventions

Intervention 1: Intervention group: To prepare Rosa syrup (according to USP 39 – NF 34, Second Supplement Commentary, June 1, 2016): 100 grams of washed Nastaran fruit soaked in 1000 cc of water, afte

Sponsors

Karaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: Men and women in the age of 35 to 65 years with high blood pressure Systolic blood pressure greater than or equal to 130 to 159 and diastolic blood pressure greater than or equal to 85 to 99 mm Hg

Exclusion criteria

Exclusion criteria: Pregnant and lactating women Patients with high normal blood pressure and grade 1 who have cardiovascular disease, especially coronary artery disease or grade 4 kidney failure or diabetes that leads to organ damage or grade 1 with chronic kidney failure grade 3 or diabetes without organ damage or organ damage due to high blood pressure The above is already specified in them. G6PD, hemochromatosis Taking medications such as warfarin, aspirin and lithium

Design outcomes

Primary

MeasureTime frame
Systolic and diastolic blood pressure. Timepoint: First visit and then every two weeks until the eighth week. Method of measurement: Digital sphygmomanometer.;Blood HDL and LDL levels. Timepoint: Beginning and end of the trial. Method of measurement: Laboratory experiment.;Severity of anxiety. Timepoint: Beginning and end of the trial. Method of measurement: Hamilton anxiety questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mina Maarefvand

Karaj University of Medical Sciences

dr.m.maarefvand@gmail.com+98 26 3464 3774

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026