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Study of Blister Fluid in Patients with Blistering Skin Diseases

Biochemical and Cytological Analysis of Blister Fluid in Autoimmune Blistering Disorders - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/03/106445
Enrollment
60
Registered
2026-03-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: L120- Bullous pemphigoid Health Condition 2: L121- Cicatricial pemphigoid Health Condition 3: L270- Generalized skin eruption due to drugs and medicaments taken internally Health Condition 4: L271- Localized skin eruption due to drugs and medicaments taken internally Health Condition 5: L20- Atopic dermatitis Health Condition 6: L23- Allergic contact dermatitis Health Condition 7: L10- Pemphigus Health Condition 8: L23- Allergic contact dermatitis Health Condition 9: L24- Irr

Interventions

Intervention1: Nil: Nil

Sponsors

Father Muller Research Center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Cases: Age more than 18 years Clinically, histopathologically, and immunologically confirmed diagnosis of PV, BP,or MMP Presence of an intact, non-infected blister less than 48 hours old No prior treatment with systemic immunosuppressants in the preceding 2 weeks Control Age more than 18 years Diagnosis of non-autoimmune and non-infectious vesiculobullous dermatoses, such as Diabetic bullae (only if diabetes is controlled), Acute eczema with vesiculation (e.g., pompholyx, allergic contact dermatitis),Friction blisters, Second-degree thermal burns Presence of intact, non-infected blister less than 48 hours old

Exclusion criteria

Exclusion criteria: Cases Infected or ruptured blisters Recent systemic steroid or immunosuppressive therapy within the last 2 weeks Severe comorbidities such as uncontrolled diabetes mellitus, renal failure, or active systemic infection Controls Clinical or immunological suspicion of autoimmune blistering disease Infective blistering conditions e.g., bullous impetigo, cellulitis with blistering Ruptured blisters Immunocompromised states e.g., HIV, malignancy, chemotherapy

Design outcomes

Primary

MeasureTime frame
To evaluate the biochemical and cytological characteristics of blister fluid in patients with autoimmune blistering disordersTimepoint: At baseline (day of presentation), prior to initiation of systemic therapy, when blister fluid is aspirated from a fresh intact blister.

Secondary

MeasureTime frame
Correlation of biochemical and cytological parameters of blister fluid with specific autoimmune blistering disorders.Timepoint: At baseline;Association of blister fluid findings with clinical characteristics of the disease (site of lesions, morphology, duration).Timepoint: At baseline

Countries

India

Contacts

Public ContactDr.Sonal Fernandes

Father Muller Medical College

sonferns007@gmail.com9606719093

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026