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Follow-up of Symptomless Inguinal and Ventral Hernias

15-year Follow-up of Laparoscopically Diagnosed Occult Inguinal and Ventral Hernias

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04683367
Acronym
hernia
Enrollment
201
Registered
2020-12-24
Start date
2003-01-01
Completion date
2020-11-30
Last updated
2020-12-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hernia, Inguinal, Hernia, Ventral, Laparoscopy

Keywords

inguinal hernia, ventral hernia, laparoscopic diagnosis

Brief summary

The orifices of all inguinal and ventral (including Spigelian) hernias were carefully recorded at the beginning of laparoscopy (n=201) of other reason (cholecystectomy, fundoplication) in 2003-5. The patients with occult hernias (n=43) were followed-up 15 years to find out what percentage of hernias would become symptomatic.

Detailed description

This was a prospective laparoscopic study of 201 consecutive adult patients operated in 2003-5. There were 133 females and 68 males with a mean age 53 ± 14 years. The index laparoscopic operation included 104 cholecystectomies, 55 fundoplications, 36 diagnostic, 5 appendectomies and one insertion of peritoneal catheter. A careful clinical examination of the groin and ventral region was performed on everybody and all patients with clinical hernias were excluded. Laparoscopic exploration of the inguinal region was considered safe and did not greatly increase the operative time. All patients were informed that hernial orifices would be explored during laparoscopy, and a written consent was asked prior to surgery. Permission to repair large hernias (\> 1 cm) was also obtained before laparoscopy. The patients were followed-up 15 years to find out, what percentage of occult, symptomless inguinal and ventral hernias were later operated because of harmfull symptoms.

Interventions

PROCEDURElaparoscopic surgery

laparoscopic repair of hernia

Sponsors

Kuopio University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* occult inguinal or ventral hernia diagnosed in laparoscopic surgery

Exclusion criteria

* clinically diagnosed inguinal or ventral hernia

Design outcomes

Primary

MeasureTime frameDescription
number of operated hernia15 yearsoccult hernia operated because of symptoms

Secondary

MeasureTime frameDescription
number of symptomatic hernia15 yearsincipient, asymptomatic hernia becomes symptomatic during follow-up

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026