Patient Satisfaction After Ingrown Toenail Surgery
1 other identifier
observational
1,200
1 country
1
Brief Summary
In this study, demographic characteristics (age, gender, which toe is involved, family history) of the patients who were operated because of ingrown nails were examined, and the post-operative satisfaction score of the patients was noted, and the recurrence rate and complications were recorded.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2021
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
September 20, 2021
CompletedFirst Submitted
Initial submission to the registry
September 21, 2021
CompletedFirst Posted
Study publicly available on registry
September 30, 2021
CompletedOctober 19, 2021
October 1, 2021
Same day
September 21, 2021
October 14, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The Surgical Satisfaction Questionnaire (SSQ-8)
SSQ-8 is a validated tool for the assessment of patients who had been operated on.
At least one year after surgery
Secondary Outcomes (3)
Recurrence
At least one year after surgery
The shape of nail clipping
through study completion, an average of 2 years
Family history
through study completion, an average of 2 years
Interventions
modified Winograd procedure
Eligibility Criteria
Patients who had ingrown toenail surgery between 8 and 80 years old.
You may qualify if:
- Patients who underwent ingrown toenail surgery Patients who could be reachable by phone over contact details on medical records
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
İstanbul Medeniyet University
Istanbul, Kadıköy, 34732, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assoc.Prof.M.D.
Study Record Dates
First Submitted
September 21, 2021
First Posted
September 30, 2021
Study Start
May 1, 2021
Primary Completion
May 1, 2021
Study Completion
September 20, 2021
Last Updated
October 19, 2021
Record last verified: 2021-10