Single site randomised trial of fibrin tissue glue versus surgery in the treatment of pilonidal sinus - Fibrin glue versus surgery for pilonidal sinus

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

EU CTR

Registry ID

EUCTR2004-002065-20-GB

Enrollment

Registered

2005-02-22

Start date

2005-03-09

Completion date

Unknown

Last updated

2019-11-25

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

Conditions

Pilonidal sinus

Interventions

Trade Name: TISSEEL kit two component fibrin sealant Pharmaceutical Form:

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - male and female subjects with pilonidal sinus - >18 years and =65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: - women who are lactating - women who are pregnant - women of childbearing age who are unwilling to take adequate contraceptive - patients with insufficient command of English to understand patient information or give informed consent

Design outcomes

Primary

Measure	Time frame
Main Objective: To compare the effectiveness of fbrin tissue glue with standard surgical techniques in the treatment of pilonidal sinus;Secondary Objective: ; Primary end point(s): - reduction in pain - healing rate - return to normal activities - recurrence of pilonidal diease - complications of glue compared to surgery	—

Countries

United Kingdom

Outcome results

None listed

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