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Effect of Roselle-based Drink on Blood Pressure and Skin

C

Chung Shan Medical University

Status

Completed

Conditions

Other Skin and Subcutaneous Infections

Treatments

Dietary Supplement: Drink

Study type

Interventional

Funder types

Other

Identifiers

NCT05084443
CS11102

Details and patient eligibility

About

This randomized, placebo-controlled, double-blind, and cross-over study was designed to check whether the roselle-based drink (2 bottles every day) can alter blood pressure and skin condition in elderly healthy subjects.

Full description

The subjects were assigned into two groups (control group and test group), each group subject was requested to drink 2 bottles every day (100 mL/bottle, one in the morning and another in the evening), the rate of drinking is 75.42%. There are 39 subjects (25 females and 14 males) completely involved in the thirteen-month trial (cross-over). Blood samples were collected at the initial, 3rd, 6th, 7th, 10th, 13th months of the trial. Skin examinations were performed at the initial, 6th, 7th, 13th months.

Enrollment

52 patients

Sex

All

Ages

40 to 81 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy adults
  • Subjects should not be under any medication
  • Subject must be able to drink

Exclusion criteria

  • Subjects with chronic renal, liver or cardiac disorders, Diabetes, hyperlipidemia.
  • Also pregnant women, chain smokers, high alcohol consumers should not be included.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

52 participants in 2 patient groups, including a placebo group

Placebo/Control
Placebo Comparator group
Description:
Placebo drink-- Orally (200 ml/day)
Treatment:
Dietary Supplement: Drink
Roselle Based drink (Test)
Experimental group
Description:
Roselle-Based Drink--- Orally (200 ml/day)
Treatment:
Dietary Supplement: Drink

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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