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Efficacy and Safety of Secukinumab in Conjunction With Surgery in Moderate to Severe Hidradenitis Suppurativa: An open-label cohort study in real clinical practice

Efficacy and Safety of Secukinumab in Conjunction With Surgery in Moderate to Severe Hidradenitis Suppurativa: An open-label cohort study in real clinical practice

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102538
Enrollment
Unknown
Registered
2025-05-15
Start date
2025-05-15
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Hidradenitis suppurativa

Interventions

Moderate to severe HS patient group:None

Sponsors

Hospital for Skin Disease, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with purulent sweat gland inflammation (HS) aged 18 (inclusive) to 80 (inclusive), with a clinical severity level of Moderate to severe (Hurley II-III grade), regardless of gender. 2. Confirmed as HS through histopathological examination by the pathology department of our hospital. 3. HS patients receiving combined surgical treatment with Sikuximab in the dermatology department of our hospital. 4. Patients with complete clinical data and a follow-up period of at least 1 year.

Exclusion criteria

Exclusion criteria: 1. Missing patients. 2. Patients who have been followed up for less than one year. 3. Patients who receive additional adjuvant therapy during the follow-up period.

Design outcomes

Primary

MeasureTime frame
HiSCR scores;IHS4 scores;The decreased number of inflammatory nodules ;The decreased number of abscess;The decreased number of sinus tracts;Reduce the degree of skin pain;The safety of the drug, paying attention to the presence of any related adverse reactions or complications;Improvement of the patient's quality of life score;

Secondary

MeasureTime frame
The onset time of the drug;The duration of the drug's therapeutic effect;Reduction of inflammatory markers (such as white blood cells, erythrocyte sedimentation rate, C-reactive protein, etc.);The convenience of drug use;Reduction of the impact on the patient's work productivity;

Countries

China

Contacts

Public ContactBu Wenbo

Hospital for Skin Disease, Chinese Academy of Medical Sciences

buwenbo@163.com+86 150 0515 7051

Outcome results

None listed

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