Skip to content

The effect of ammonium lactate 14% and IPL on keratosis pilaris

Clinical trial of comparing the effect of ammonium lactate 14% and IPL versus ammonium lactate 14%-alone on keratosis pilaris

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016061428448N1
Enrollment
50
Registered
2016-12-07
Start date
2016-01-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Keratosis pilaris. Other specified epidermal thickening

Interventions

Intervention 1: Control group receives topical ammonium lactate 14% making the company noreva twice a day used as a thin layer on the waste for 3 months. Intervention 2: In treatment group
Treatment - Other
Control group receives topical ammonium lactate 14% making the company noreva twice a day used as a thin layer on the waste for 3 months.
In treatment group we done 3 IPL sessions with 4 weeks interval and also advised the patients to apply topical ammunium lactate 14% making the company noreva twice a day used as a thin layer on the wa

Sponsors

Vice Chancellor foer research of Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria:being afflicted with keratosis pilaris; patients who don't tend to only longterm and topical treatment and they prefer laser treatmen; no pregnancy and breast feeding and consent to participate in the study. Exclusion criteria:sensitivity to Ammonium lactate; no regular visits and using cotreatments.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical improvment. Timepoint: Before, 1 month after final treatment and 2 month after final treatment. Method of measurement: Photography evaluation by two blinded dermatologist.

Secondary

MeasureTime frame
Improvements Vas score. Timepoint: Before, 1 month after final treatment and 2 month after final treatment. Method of measurement: Question from patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSiamak Rahmani

Isfahan University of Medical Science

siamak.dermatologist@gmail.com+98 31 3627 2548

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026