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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00226161
Other study ID # 171178
Secondary ID
Status Terminated
Phase N/A
First received September 22, 2005
Last updated January 25, 2013
Start date September 2005
Est. completion date September 2013

Study information

Verified date September 2005
Source University Hospital, Gentofte, Copenhagen
Contact n/a
Is FDA regulated No
Health authority Denmark: The Danish National Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether laparoscopic inguinal hernia repair leads to a lower incidence of chronic pain compared to open herniorrhaphy.


Recruitment information / eligibility

Status Terminated
Enrollment 0
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers
Gender Male
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Primary inguinal hernia

Exclusion Criteria:

- History of severe mental illness or chronic pain elsewhere

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Procedure:
Inguinal herniorrhaphy


Locations

Country Name City State
Denmark Department of Surgical Gastroenterology, Gentofte University Hospital, Hellerup

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Gentofte, Copenhagen

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Chronic pain
Secondary Recurrence of the hernia
See also
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Active, not recruiting NCT04328597 - Portuguese Inguinal Hernia Cohort (PINE) Study
Completed NCT04033055 - Antalgic Efficacy of CycloMeshâ„¢ Soaked in Ropivacaine Hydrochloride in Uncomplicated Inguinal Hernia. N/A
Completed NCT03590145 - Reliability of the Doha Agreement Classification of Groin Pain