- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05062616
Patient Satisfaction After Ingrown Toenail Surgery
Patient Satisfaction After Ingrown Toenail Surgery. A Review of 1200 Cases
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Kadıköy
-
Istanbul, Kadıköy, Turkey, 34732
- İstanbul medeniyet University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Patients who underwent ingrown toenail surgery Patients who could be reachable by phone over contact details on medical records
Exclusion Criteria:
Patients who were not reachable Patients who underwent another surgery on the targeted foot rather than ingrown toenail surgery Patients who had fractures on the targeted foot Clinical diagnosis of Alzheimer disease or patients who have lost their cognitive functions.
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Surgical Satisfaction Questionnaire (SSQ-8)
Time Frame: At least one year after surgery
|
SSQ-8 is a validated tool for the assessment of patients who had been operated on.
|
At least one year after surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Recurrence
Time Frame: At least one year after surgery
|
Recurrence rate is noted
|
At least one year after surgery
|
The shape of nail clipping
Time Frame: through study completion, an average of 2 years
|
straight or round cut
|
through study completion, an average of 2 years
|
Family history
Time Frame: through study completion, an average of 2 years
|
Positive or negatif family history
|
through study completion, an average of 2 years
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021-03
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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