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The efficacy and safety of 0.5% topical timolol on corneometry and transepidermal water loss after ablative fractional CO2 laser for atrophic acne scars: a split face randomized double blind placebo-controlled trial

The efficacy and safety of 0.5% topical timolol on corneometry and transepidermal water loss after ablative fractional CO2 laser for atrophic acne scars: a split face randomized double blind placebo-controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190722005
Enrollment
25
Registered
2019-07-22
Start date
2019-07-22
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

We considered that timolol may have an effect in wound healing promotion in patients who undergo AFCO2 resurfacing. Our study aimed to investigate the efficacy and safety of 0.5% topical timolol malea

Interventions

timolol&#44
which is non&#45
selective beta blocker&#44
could promote the keratinocyte migration rate via mitogen&#45
activated protein kinase signaling pathway and accelerate the wound healing rate.
Active Comparator Drug
0.5% timolol maleate

Sponsors

none
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: The participants aged 18-50 years old with atrophic area scars for at least three months

Exclusion criteria

Exclusion criteria: 1) pregnant/lactating female, 2) history of isotretinoin use within previous 3 months before enrollment, 3) history of cosmetic procedures including botulinum toxin, filler, collagen, lasers within the preceding 3 months, 4) history of photosensitivity or skin cancer, 5) history of psoriasis, hypertension, or asthma, 6) allergy to anesthetic agents, or timolol solution, 7) active dermatitis or herpes infection (within previous 2 weeks), 8) Fitzpatrick skin type V – VI, 9) current or history of previous use within one month of anticoagulative drugs or NSAIDs use or previous use

Design outcomes

Primary

MeasureTime frame
corneometry and TEWL - biophysical measurements by Cutometer dual MPA 580

Secondary

MeasureTime frame
edema, erythema, and crusting score - 4-point grading scale by dermatologists

Countries

Thailand

Contacts

Public ContactChanat Kumtornrut

Chulalongkorn University

chanat_1@yahoo.com668-1459-4965

Outcome results

None listed

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