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Endoscopic Pilonidal Sinus Treatment (EPSiT) For Sacrococcygeal Pilonidal Sinus Disease: A Prospective Long-Term Study

Endoscopic Pilonidal Sinus Treatment (EPSiT) For Sacrococcygeal Pilonidal Sinus Disease: A Prospective Long-Term Study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073698
Enrollment
Unknown
Registered
2023-07-19
Start date
2014-07-01
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

pilonidal sinus

Interventions

Experimental group:Endoscopic Pilonidal Sinus Treatment (EPSiT)

Sponsors

Shifa international hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 51 Years

Inclusion criteria

Inclusion criteria: All patients presenting to the Outpatients with pilonidal sinus with or without abscess will be included in the study

Exclusion criteria

Exclusion criteria: Only failure to give consent will be excluded

Design outcomes

Primary

MeasureTime frame
Wound infection;Visual analogue scale;

Secondary

MeasureTime frame
Recurrence at 6 months to 1 year after surgery;Time taken to return at work ;Patient satisfaction in terms of quality of life, mobility;

Countries

pakistan

Contacts

Public ContactMuhammad Amir

Shifa international hospital; Shifa college of medicine

mamir99@yahoo.com0923215113460

Outcome results

None listed

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