Actively Recruiting

Phase Not Applicable
Age: 12Years - 75Years
All Genders
NCT07547241

Comparison of Two Surgical Methods (Winograd vs. Sleeve Method) in the Treatment of Ingrown Toenail.

Led by Pakistan Institute of Medical Sciences · Updated on 2026-04-23

312

Participants Needed

1

Research Sites

60 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized clinical trial aims to compare the recurrence rates of two surgical techniques-Winograd procedure and sleeve (gutter) method-in the treatment of ingrown toenails (onychocryptosis). A total of 312 nails will be randomized into two groups, with patients receiving either the Winograd procedure or sleeve method. Participants will be followed for 30 days post-intervention to assess recurrence and other clinical outcomes. The study seeks to determine the more effective treatment modality for reducing recurrence in a tertiary care setting.

CONDITIONS

Official Title

Comparison of Two Surgical Methods (Winograd vs. Sleeve Method) in the Treatment of Ingrown Toenail.

Who Can Participate

Age: 12Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients presenting with ingrown toenail (onychocryptosis)
  • Patients for whom surgical intervention is indicated
  • Age between 12 and 75 years
  • Both male and female participants
  • Patients willing to provide informed consent
Not Eligible

You will not qualify if you...

  • Patients with diabetes mellitus
  • Patients with peripheral vascular disease
  • Immunocompromised patients
  • Patients with coagulopathy
  • Patients receiving chemotherapy
  • Patients with localized infection or abscess at the surgical site
  • Patients with previously treated or recurrent ingrown toenail
  • Patients presenting with delayed complications of prior ingrown toenail surgery

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Pakistan Institute of Medical Sciences

Islamabad, Pakistan, 29111

Actively Recruiting

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Research Team

M

Muhammad Fahad Ali, MBBS, MRCS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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