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CompletedPhase 3

Efficacy of Oral Tofacitinib in Moderate to Severe Alopecia Areata, Totalis and Universalis at Tertiary Care Hospital, Karachi.

Key facts

Who runs it
Jinnah Hospital
Where
Pakistan1 site in 1 countryChoose a country to see its sites
Trial code
Status
Completed
Phase
Phase 3
People taking part
30 people enrolled
Started
1 Jul 2023
Ended
16 Jan 2024
Type of study
Interventional
Treatments tested
  • Tofacitinib
Record updated
26 February 2024

Who can take part

Age
15 years to 60 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 7 criteriaShow less

Who can take part

  • Patients presenting with Alopecia areata as per operational definition will be included in the study
  • Either gender
  • Age 15 - 60 years

Who cannot take part

  • Patients having history of treatment with systemic agents, having active infection, pregnant and lactating women and patients having severe hematological abnormalities
  • Patient with history of connective tissue disorders, vasculitis, seropositive and seronegative arthritis
  • Patients positive for latent infections
  • Patients with weight <25 kg

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

To determine the efficacy of oral Tofacitinib in the treatment of moderate to severe alopecia areata, totalis and universalis at tertiary care hospital of Karachi, Pakistan. Efficacy of treatment in patients presenting with alopecia areata will be assessed using SALT Score on follow up at 6,12 and 24 weeks where four categories of treatment response were defined: 0 (re-growth ≤10%), 1 (11-25%), 2 (26-50%), 3 (51-75%) and 4 (re-growth >75%). Efficacy will be considered if re-growth ≥ 2.

The group in the trial

  • TofacitinibTreatment being tested

    tofacitinib 5mg twice daily for 6 months

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Record updated
26 February 2024