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St. John's Wort Photodynamic Therapy

Not Applicable
Completed
Conditions
Acne
Interventions
Procedure: PDT
Registration Number
NCT05073211
Lead Sponsor
Seoul National University Bundang Hospital
Brief Summary

The investigators aimed to evaluated the efficacy and safety of SJW-PDT compared to indole-3-acetic acid (IAA)-PDT in the treatment of acne. The investigators also investigated the skin rejuvenating effects of SJW-PDT.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
31
Inclusion Criteria
  • patients with mild to moderate facial acne
  • between 25 and 60 years old
Exclusion Criteria
  • history of oral retinoid treatment with the past 6 months
  • history of oral antibiotics, topical acne treatment, or skin rejuvenation treatment such as lasers and chemical peeling within the month before the start of the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
SJW-PDTPDTParticipants were randomized to receive either the SJW extract or IAA on each split-face. The SJW extract (DR-Light complexTM; Genicos Co., Ltd, Cheongju, Korea) consisted of 70% 1, 3-butylene glycol, and 0.1% hypericin as active ingredients. After cleansing the face gently, participants applied 1.5 ml of 0.5% SJW extract on one half of the face and 1.5 ml of 0.015% IAA (AC gel®; Wellskin, Seoul, Korea) on the other half of the face for 10 minutes under occlusion.
IAA-PDTPDTParticipants were randomized to receive either the SJW extract or IAA on each split-face. The SJW extract (DR-Light complexTM; Genicos Co., Ltd, Cheongju, Korea) consisted of 70% 1, 3-butylene glycol, and 0.1% hypericin as active ingredients. After cleansing the face gently, participants applied 1.5 ml of 0.5% SJW extract on one half of the face and 1.5 ml of 0.015% IAA (AC gel®; Wellskin, Seoul, Korea) on the other half of the face for 10 minutes under occlusion.
Primary Outcome Measures
NameTimeMethod
acne lesions1 and 4 weeks after the last treatment

change in the number of acne lesions after the treatment

Secondary Outcome Measures
NameTimeMethod
sebum secretion rate (μg/cm2)1 and 4 weeks after the last treatment

Sebum secretion rate was measured with Sebumeter SM 815®.

Trial Locations

Locations (1)

Seoul National University Bundang Hospital

🇰🇷

Seongnam, Korea, Republic of

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