Skip to content

Efficacy of needling with topical 1% celecoxib cream in the treatment of Keloidal

Efficacy of needling with topical 1% celecoxib cream in the treatment of Keloidal.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240321061344N1
Enrollment
25
Registered
2024-04-10
Start date
2024-04-20
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Keloid. Hypertrophic scar

Interventions

Intervention group: Every two weeks for 3 months, using a fine 50cc insulin syringe head, first needling was performed on the keloid lesions (lesions anywhere on the body except the face and genital a

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: Individuals with a clinical diagnosis of primary keloid by a dermatological specialist 15 years of age and older who volunteer to participate in this research Individuals who have not received any treatment for keloid lesions and in case of previous treatment, at least 3 months from Colloidal lesions on the trunk, limbs, back and hips

Exclusion criteria

Exclusion criteria: The presence of skin disease around the selected keloid lesion for treatment, such as various types of dermatitis and infectious and fungal diseases Pregnancy Breastfeeding Colloidal lesions on the face and genitals History of recent scar treatment (less than 3 months have passed since his treatment) Background of previous drug sensitivity to NSAIDs

Design outcomes

Primary

MeasureTime frame
Keloid score in POSAS questionnair. Timepoint: At the beginning of the study and 3 months after the start of the study. Method of measurement: The patient and observer Scar Assessment scale/Dermoscopy.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVahid Mashayekhiquyonlu

Mashhad University of Medical Sciences

Mashayekhiv@mums.ac.ir+98 51 3851 3400

Outcome results

None listed

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