Tissue coverage in axillary hidradenitis suppurativa

Comparison of split thickness skin grafts and flaps in bilateral chronic axillary hidradenitis suppurativa: a prospective clinical trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20191019045155N2

Enrollment

Registered

2020-01-23

Start date

2010-03-01

Completion date

Unknown

Last updated

2020-02-24

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

Conditions

Axillary hidradenitis suppurativa. Hidradenitis suppurativa

Interventions

Intervention group: One group of 30 patients that received split thickness graft on left side and flap on right side after debridement of chronic bilateral axillary hidradenitis suppurative. The graf

Eligibility

Sex/Gender

Male

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: ???Age between 18 and 70 years old Diagnosis of bilateral axillary hidradenitis suppurativa American Society of Anesthesiology classes of I and II Having informed consent to enter the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Complete recovery of the sides of graft and flap. Timepoint: The patients were followed-up for one year and then were visited on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: by visiting the patients and examining.;Recurrence. Timepoint: The patients were followed-up for one year and then were visited on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: by visiting the patients and examining.;Patient's satisfaction. Timepoint: The patients were followed-up for one year and then were visited on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: by visiting the patients and examining.;Range of motion of the shoulder. Timepoint: The patients were followed-up for one year and then were visited on on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: by visiting the patients and examining.;Pain on side or region of the flap or graft. Timepoint: The patients were followed-up for one year and then were visited on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: Universal Pain Assessment Tool (UPAT).	—

Measure

Time frame

Complete recovery of the sides of graft and flap. Timepoint: The patients were followed-up for one year and then were visited on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: by visiting the patients and examining.;Recurrence. Timepoint: The patients were followed-up for one year and then were visited on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: by visiting the patients and examining.;Patient's satisfaction. Timepoint: The patients were followed-up for one year and then were visited on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: by visiting the patients and examining.;Range of motion of the shoulder. Timepoint: The patients were followed-up for one year and then were visited on on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: by visiting the patients and examining.;Pain on side or region of the flap or graft. Timepoint: The patients were followed-up for one year and then were visited on a regular basis. At first one month after surgery then three, six and twelve months after their second operation. Method of measurement: Universal Pain Assessment Tool (UPAT).

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbolfazl Afsharfard

Shahid Beheshti University of Medical Sciences

pr_shohada@sbmu.ac.ir+98 21 25719

Outcome results

None listed

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