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Clinical Trials/NCT06854419
NCT06854419CompletedNot Applicable

Efficacy Evaluation of Blood Peach Extract and Rose Apple Extract on Skin

TCI Co., Ltd.1 site in 1 country75 target enrollmentStarted: April 7, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
75
Locations
1
Primary Endpoint
the volume of skin wrinkles

Study Overview

Brief Summary

Evaluate the effects of blood peach extract drink and rose apple extract drink on enhancing hemoglobin and iron levels, and improving skin health.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
20 Years to 65 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Healthy adult females aged 20 to 65;
  • •Preferably those with pale complexion or signs of iron deficiency anemia.

Exclusion Criteria

  • •Currently undergoing or having undergone any medical beauty treatments within the past month (including skincare, laser treatments, chemical peel, injections, or cosmetic surgery);
  • •Outdoor workers (exposed to sunlight for more than 5 hours daily);
  • •Pregnant, breastfeeding, or planning to become pregnant during the trial (self-reported);
  • •Individuals with heart, liver, kidney, endocrine, or other significant organic diseases (self-reported);
  • •Individuals who have undergone major surgery (according to medical history);
  • •Long-term medication users;
  • •Individuals with mental health disorders;
  • •Those who are already regularly taking iron supplements;
  • •Faculty or staff members who are currently enrolled in the principal investigator's courses.

Arms & Interventions

Placebo

Placebo Comparator

Intervention: Placebo Drink (Dietary Supplement)

Blood Peach Extract

Experimental

Intervention: Blood Peach Extract Drink (Dietary Supplement)

Rose Apple Extract

Experimental

Intervention: Rose Apple Extract Drink (Dietary Supplement)

Outcomes

Primary Outcomes

the volume of skin wrinkles

Time Frame: Volume change from Baseline skin wrinkles at 8 weeks

IRV full-face skin analyzer was utilized to measure skin wrinkles. Units: arbitrary units

the roughness of skin texture

Time Frame: Rating skin roughness from Baseline skin texture at 8 weeks

IRV full-face skin analyzer was utilized to measure skin texture. Units: arbitrary units

Secondary Outcomes

  • the change of Total Iron Binding Capacity (TIBC) level of blood(Change from Baseline TIBC level at 8 weeks)
  • the change of unsaturated iron-binding capacity (UIBC) level of blood(Change from Baseline UIBC level at 8 weeks)
  • the change of skin collagen density(Change from Baseline skin collagen density at 8 weeks)
  • the change of skin elasticity(Change from Baseline skin elasticity at 8 weeks)
  • the change of skin pores(Change from Baseline skin pores at 8 weeks)
  • the change of skin tone(Change from Baseline skin tone at 8 weeks)
  • the change of skin hydration(Change from Baseline skin hydration at 8 weeks)
  • the change of skin melanin/erythema index(Change from Baseline skin melanin/erythema index at 8 weeks)
  • the change of skin redness(Change from Baseline skin redness at 8 weeks)
  • the change of lip redness(Change from Baseline lip redness at 8 weeks)
  • the change of Red Blood Cells (RBC) Count of blood(Change from Baseline RBC count at 8 weeks)
  • the change of mean corpuscular volume (M.C.V) level of blood(Change from Baseline M.C.V level at 8 weeks)
  • the change of mean corpuscular hemoglobin concentration (M.C.H.C) level of blood(Change from Baseline M.C.H.C level at 8 weeks)
  • the change of ferrous level of blood(Change from Baseline ferrous level at 8 weeks)
  • the change of ferritin level of blood(Change from Baseline ferritin level at 8 weeks)
  • the change of hemoglobin level of blood(Change from Baseline hemoglobin level at 8 weeks)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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