We updated the design of this site on December 18, 2017. Learn more.
ClinicalTrials.gov Menu

Chronic Pain After Inguinal Herniorrhaphy

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00226161
Recruitment Status : Terminated
First Posted : September 26, 2005
Last Update Posted : January 28, 2013
Information provided by:
University Hospital, Gentofte, Copenhagen

Brief 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.

Condition or disease Intervention/treatment
Inguinal Hernia Procedure: Inguinal herniorrhaphy

Study Type : Interventional  (Clinical Trial)
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Primary Purpose: Prevention
Study Start Date : September 2005
Estimated Primary Completion Date : September 2013
Estimated Study Completion Date : September 2013

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Chronic Pain Hernia
U.S. FDA Resources

Primary Outcome Measures :
  1. Chronic pain

Secondary Outcome Measures :
  1. Recurrence of the hernia

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   Male

Inclusion Criteria:

  • Primary inguinal hernia

Exclusion Criteria:

  • History of severe mental illness or chronic pain elsewhere

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00226161

Department of Surgical Gastroenterology, Gentofte University Hospital,
Hellerup, Denmark, 2900
Sponsors and Collaborators
University Hospital, Gentofte, Copenhagen
Study Director: Jacob Rosenberg, professor,dr.med,chief consul Gentofte University Hospital

ClinicalTrials.gov Identifier: NCT00226161     History of Changes
Other Study ID Numbers: 171178
First Posted: September 26, 2005    Key Record Dates
Last Update Posted: January 28, 2013
Last Verified: September 2005

Additional relevant MeSH terms:
Hernia, Inguinal
Hernia, Abdominal
Pathological Conditions, Anatomical