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10-year Results of Open Inguinal Hernia Repair

CompletedNCT06008535
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The main goal of the research is to evaluate the long-term results of open anterior alloplasty of inguinal hernia, mainly the occurrence of recurrences. The secondary aim of the study is to clarify the incidence of chronic pain and foreign body sensation 10 years after inguinal hernia surgery. Patients who meet the criteria for inclusion in the study are invited to an appointment, where a questionnaire is filled out, an clinical examination and an ultrasound examination are performed.

Study details

Official title
10-year Results of Open Inguinal Hernia Repair. A Prospective Study
Conditions
Interventions
  • Procedure: Open inguinal hernia repair
Sponsor
Tartu University Hospital
Start date
2018-05-22
Primary completion
2023-12-31
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
Estonia
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * primary inguinal hernia operated between 2008-2013 at the Tartu University Hospital * elective surgery * age at least 18 years old at the time of the operation * ability to understand the guidelines and willing to participate in the study Exclusion Criteria: * recurrent hernia * strangulated hernia * age under 18 years at the time of surgery * does not agree to participate in the study * does not understand the guidelines. Regarding the last exclusion criterion: since it is an assessment of the remote results of the treatment and probably relatively many of the subjects are very elderly, it may happen that when contacting the patient by phone it turns out that the patient is no longer adequate to make a decision about participating in the study or to answer questions (experienced cerebral infarction, dementia, etc. .) - in this case, the patient is not invited to the appointment.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06008535