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Comparative Study for Treatment of Alopecia Areata Using Carboxytherapy and Intralesional Steroids

K

Kasr El Aini Hospital

Status and phase

Unknown
Phase 4

Conditions

Alopecia Areata

Treatments

Device: Carboxytherapy
Drug: Intralesional Steroid Injection

Study type

Interventional

Funder types

Other

Identifiers

NCT04228029
KasrEliniH

Details and patient eligibility

About

Patients with three lesions of alopecia areata are randomly recruited in this study. Each lesion is randomized in to receiving either carboxytherapy in one lesion, intralesional steroids in another lesion and combination of both in the third lesion.

Treatment period is 3 months followed by a follow-up period of 2 months.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • early localized scalp alopecia areata
  • patients who did not receive any medication for at least 2 months before starting the study Patients who agreed to join the study and signed written consent.

Exclusion criteria

  • pregnant, and lactating females and those with unrealistic expectation.
  • Alopecia totalis or universalis or ophiasis or cicatrising alopecia
  • Usage of systemic treatment of alopecia areata 2 months prior to the study.
  • Any scalp lesion within the treated area
  • Bleeding diathesis, severe anemia or platelet disorders
  • Medical conditions such as autoimmune diseases.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

Double Blind

30 participants in 3 patient groups

Carboxytherapy
Active Comparator group
Treatment:
Device: Carboxytherapy
Intralesional steroids
Active Comparator group
Treatment:
Drug: Intralesional Steroid Injection
Combination of carboxytherapy and intralesional steroids
Active Comparator group
Treatment:
Drug: Intralesional Steroid Injection
Device: Carboxytherapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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