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A Study Comparing The Efficacy and Safety of Jessner's Solution And Salicylic Acid 30% Chemical Peel and in the Management of Acne Vulgaris and Post Acne Hyperpigmentation

Efficacy and safety of Jessner’s Solution peel (JS) in comparison with Salicylic Acid 30% peel (SA) in management of patients with acne vulgaris and post acne hyperpigmentation: A randomized, double-blinded, split-face, controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190118001
Enrollment
Unknown
Registered
2019-01-18
Start date
2018-10-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Acne Vulgaris Post Acne Hyperpigmentation Acne Vulgaris Post Acne Hyperpigmentation

Interventions

Jessner’s Solution is a chemical containing salicylic acid&#44
lactic acid and resorcinol that has been used in the market for decades&#44
especially in the field of dermatology and aesthetic.,Salicylic acid had been known to be lipophilic and had anti&#45
inflammatory properties. Its efficacy in the treatment of acne vulgaris is well established
Experimental Device,Active Comparator Device
Jessner&#39
s Solution,Salicylic Acid 30%

Sponsors

Dermatological Society of Malaysia
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Males and females with acne vulgaris aged ≥ 18 years old 2. Should have at least 10 inflammatory AND/ OR non-inflammatory lesions at each side of the face 3. Have acne for more than 6 months

Exclusion criteria

Exclusion criteria: 1. Other forms of acne (acne conglobata, acne excoriate, acne rosacea, acne cosmetica, pomade acne, acne fulminans, acne keloidalis nuchae, acne chloracne, acne mechanica and acne medicamentosa) 2. Nodulocystic acne 3. On oral antibiotic for the last 1 months 4. On oral isotretinoin for the last 6 months 5. On topical antimicrobial or tretinoin for the last 2 weeks 6. Photosensitivity 7. Recent (2-6months) facial undermining surgery (blepharoplasty, rhytidectomy, brow lift, liposuction) in the treatment area 8. If there is any active or past infection, such as HSV, herpes zoster infection 9. If there is any active bacterial folliculitis at this moment 10. History of keloid 11. Poor skin turgor 12. If patient is currently pregnant or lactating 13. Other comorbidities, especially immunocompromising diseases (possibility of dealy healing, increased susceptibility to infection, or excessive pigmentation after peeling) 14. If there is any known allergy to the active ingredients in the preparation 15. Patients who have any other dermatoses, especially facial dermatoses 16. Patients who like outdoor activities and couldn’t comply to sunprotection. 17. Fitzpatrick skin type I-II 18. Patients who had a difference of 2 grades or above, comparing one side of the face to another.

Design outcomes

Primary

MeasureTime frame
Changes in total number of inflammatory lesions and non-inflammatory lesions. At each clinic visit lesions count

Secondary

MeasureTime frame
Changes in the Michaelson Acne Score (MAS) At each clinic visit Michaelsson Acne Score,Changes in post acne hyperpigmentation index (PAHPI) at each clinic visit PAHPI,The patient’s satisfactory rate towards the treatment Last clinic visit Visual Analogue Scale,The frequency of overall all adverse reaction towards the treatment At each clinic visit Frequency

Countries

Malaysia

Contacts

Public ContactKang Nien How

Faculty of Medicine and Health Sciences, Universiti Putra Malaysia

hkangnien@upm.edu.my(+60) 0389472568

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026