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Completed

NCT Number: NCT00683098

Long-term Results After Endoscopic Total Extraperitoneal Repair of Recurrent Inguinal Hernia

Evaluation of long-term results for chronic pain and impairment of daily activities after endoscopic total extraperitoneal repair of recurrent inguinal hernia with inguinal pain questionnaire (IPQ).

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

St. Claraspital

Basel, 4019, Switzerland

About this study

Evaluation of long-term results for chronic pain and impairment of daily activities after endoscopic total extraperitoneal repair of recurrent inguinal hernia with inguinal pain questionnaire (IPQ).

All patients, who had a endoscopic preperitoneal mesh repair of a recurrent inguinal hernia between 1995 and 2008 were prospectively recorded and will be sent the IPQ via mail.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients, who had endoscopic total extraperitoneal repair of recurrent inguinal hernia at our institution between 1995 and 2008

Exclusion criteria

  • none

Treatment and study plan

Primary outcomes

  1. Pain according to Inguinal Pain Questionnaire Activity according to Inguinal Pain Questionnaire

    Time frame: up to 10 years

Secondary outcomes

  1. Recurrence, Reoperation

    Time frame: up to 10 years

Sponsors and collaborators

Lead sponsor

St. Claraspital AG

Other

Registry information

Important dates

Study start
2008
Primary completion
2008
Study completion
2008
First posted
May 23, 2008
Registry last updated
Apr 18, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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