CClinicalTrials.gg
Status unknownNCT02126657Updated Apr 30, 2014

The Efficacy and Safety of a Single 70% Glycolic Acid Peel With Vitamin C for the Treatment of Acne Scars

A Phase 2 interventional study of 70% glycolic acid in Acne Scars, sponsored by National University Hospital, Singapore. Status unknown at 1 site in Singapore. Open to participants aged 21 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2014-04-30.

Sponsored by National University Hospital, Singapore · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Apr 2014), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
21 Years to 60 Years
Sex
All
01

Study summary

Our study involves the evaluation of a high potency chemical peel in its efficacy and safety profile for the treatment of acne scars. This chemical peel regime is a high potency peel of 70% glycolic acid combined with vitamin C that is purported to provide a good balance between yielding results and patient safety. We aim to evaluate its efficacy and safety profile of a single application. The study design is based on a single group that compares pre- vs post-intervention. 10 patients with atrophic acne scars of skin type I-IV will be recruited. Potential benefits include improvement of post acne scars with a short downtime and risks include post peel hyper pigmentation and scarring. We believe that this treatment will be highly beneficial to patients with post acne scarring.

This chemical peel regime has good efficacy and safety profile for the treatment of acne scars.

Read the detailed description

Primary endpoints:

  1. ECCA (échelle d'évaluation clinique des cicatrices d'acné) grading scale for quantitative grading of acne scars. Two blinded evaluators compare and rate the photograph using ECCA score.
  2. Patient Assessment Based on 1 to 10 point scale; 1- nil acne scars and 10- severe acne scar

Secondary endpoints:

  1. Postacne hyperpigmentation index (PAHPI)

    -Each of these 3 variables --size, intensity, and number of lesions is weighted and the summation of the weighted variables gives the total PAHPI score, ranging 6 to 22.

  2. Safety Assessment (This is an ordinal scale) i. Score of redness ii. Score of swelling iii. Score of oozing/crusting iv. Post peel hyperpigmentation v. Post peel scarring vi. Assessment based on patient and doctor global assessment (global assessment from 1 - 10)
02

Conditions studied

  • Acne Scars

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Keywords

  • Acne scars
  • 70% Glycolic acid peel
03

In context

Acne Vulgaris

730 studies on the registry are indexed under Acne Vulgaris; 86 are open to participants now.

This study's planned enrollment of 10 is below the median of 69 across 628 interventional studies indexed under Acne Vulgaris.

Browse Acne Vulgaris studies →

Lead sponsor

National University Hospital, Singapore is the lead sponsor of 444 studies on the registry; 96 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Atrophic scars
  2. Skin type I to IV

Exclusion criteria

Exclusion Criteria:

  1. Pregnancy, breastfeeding
  2. Active dermatitis (on the face), rosacea, allergic rhinitis, active herpes simplex
  3. Known hypersensitivity
  4. Previous keloids
  5. Laser ablative procedures within the last month
  6. Chemical peels within the last 6 months
  7. Used oral retinoids in the past 6 months
  8. Used topical retinoids in the past one week
  9. Used scrub, AHA, skin irritant for the past 24h
  10. Presence of facial warts or fungal infections
  11. Photoallergies
  12. Prior poor reaction to a chemical peel
  13. Radiotherapy
  14. Skin type V and VI
  15. Patients with predominantly ice pick and boxcar scars
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Other
    Single Arm

    Single arm study - pre and post peel assessment

    Drug: 70% glycolic acid

Interventions

  • Drug70% glycolic acid
06

What researchers measure

Primary outcomes

  1. Efficacy Assessment

    1. ECCA (échelle d'évaluation clinique des cicatrices d'acné) grading scale for quantitative grading of acne scars * V-shaped atrophic scars with diameter \<2 mm: 15 * U-shaped atrophic scars with a diameter of 2-4 mm: 20 * M-shaped atrophic scars with diameter \>4 mm: 25 * Superficial elastolysis: 30 * Hypertrophic scars with a \<2-year duration: 40 * Hypertrophic scars of \>2-year duration: 50 A semi-quantitative scoring of number of each scar will be performed * No scars: 0 * Less than five scars: 1 * Between five and 20 scars: 2 * More than 20 scars: 3 2. Patient Assessment Based on 1 to 10 point scale; 1- nil acne scars and 10- severe acne scar Secondary endpoints 1) Postacne hyperpigmentation index (PAHPI)

    Time frame: 3 months

  2. Safety Assessment

    ) Safety Assessment (This is also an ordinal scale) i. Score of redness ii. Score of swelling iii. Score of oozing/crusting iv. Post peel hyperpigmentation v. Post peel scarring

    Time frame: 3 months

07

Study locations

1 site
  • National University Hospital
    Singapore, 119074, Singapore
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 30, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02126657
Lead sponsor
National University Hospital, Singapore
Responsible party
Sponsor
First posted
Apr 30, 2014
Start date
May 2014
Primary completion
Nov 2014 (estimated)
Completion
Nov 2014 (estimated)
Last update
Apr 30, 2014

Study contacts

Sam SY Yang, Dr
Contact
samsyyang@gmail.com
85333992

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2014. You cannot join it, but the record below documents what was studied.

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