Comparison between Sorbsan silver dressing and traditional dressing in wound healing of operated Pilonidal sinus

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT201405288375N8

Enrollment

Registered

2014-07-21

Start date

2014-04-04

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Pilonidal sinus. Pilonidal cyst with abscess

Interventions

Intervention 1: Control: Traditional wound dressing. Intervention 2: Intervention: Sorbsan silver dressing.

Treatment - Other

Control: Traditional wound dressing

Intervention: Sorbsan silver dressing

Eligibility

Sex/Gender

All

Age

17 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age 18 to 40 years; Body mass index (BMI) less than 35; agreement to participate in the study Exclusion criteria: Chronic disease (diabetes mellitus, anemia, malnutrition, immune compromised disease); drug history (corticosteroids, chemotherapy, radiotherapy); age more than 40 years

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Wound healing. Timepoint: Each 72h until granulation tissue formation. Method of measurement: Percent.	—

Secondary

Measure	Time frame
Pain severity. Timepoint: Each 72 h until granulation tissue formation. Method of measurement: Visual Analogue Scale.;Time to return to activity. Timepoint: Each 72 h until granulation tissue formation. Method of measurement: Day.;Infection rate. Timepoint: Each 72 h until granulation tissue formation. Method of measurement: Observation.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Ghodrat Allah Naseh

Surgery ward, Emam Reza Educational Hospital, Birjand University of Medical Sciences

Nasehghodrat@yahoo.com+98 56 1222 2300

Outcome results

None listed

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