Altering Toenail Biomechanic in Managing Ingrown Toenail.

Ingrown Toenail Clinical Trial

Official title:

Altering Toenail Biomechanic in Managing Ingrown Toenail.Randomized Clinical Trial.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03732313
• Other study ID #: 27908201300677
• Status: Completed
• Phase: N/A
• Start date: January 1, 2017
• Est. completion date: July 1, 2018

Study information

• Verified date: November 2018
• Source: Zagazig University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Ingrown toenail is commonly met in clinical practice.treatment may be non-operative and operative treatment.operative trestment depends on lateral wedge resection of the nail. The idea is to change toenail biomechanics by central toenail resection.

Description:

The aim of this study is to compare between central toenail resection with ordinary lateral wedge resection in managing ingrown toenail. This study was performed on 100 patients divided into 2 groupd each is 50 patients. Group A underwent central resection while group B underwent lateral toenail resection.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: July 1, 2018
• Est. primary completion date: January 1, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 10 Years to 35 Years

Eligibility

Inclusion Criteria:

• patient with ingrown toenail

• Patients from 10 years up to 35 years

Exclusion Criteria:

• patients with concurrent toe deformity

• patients less than 10 years or more than 35 years

Related Conditions & MeSH terms

• Ingrown Toenail
• Nails, Ingrown

Intervention

Procedure:
• Central toenail resection
Using local aneasthesia, resection of central part of toenail with germinal matrix.
• Wedge toenail resection
Using local anaesthesia,we remove lateral part of toenail .

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Zagazig University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Postoperative pain on visual analog score for pain	All patients are pain free after 5 days postoperative	six month
Primary	Intraoperative time measured in minutes	All operations end within 15 minutes.	Six month
Secondary	Recurrence after operation	Recurrence is followed up by asking the patient to follow up in outpatient clinic after six month and also,by calling the patients in telephone.	six month