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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01085110
Other study ID # H-2-2009-126-A
Secondary ID
Status Completed
Phase N/A
First received March 10, 2010
Last updated May 29, 2012
Start date January 2010
Est. completion date May 2010

Study information

Verified date May 2012
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Dataprotection AgencyDenmark: Ethics Committee
Study type Observational

Clinical Trial Summary

Describe and characterizes laparoscopic postherniotomy patients with persistent moderate/severe pain affecting every day activities - including detailed quantitative sensory assessment


Recruitment information / eligibility

Status Completed
Enrollment 11
Est. completion date May 2010
Est. primary completion date April 2010
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Male patients > 18 yrs

- No sign of hernia recurrence

- Chronic groin pain lasting more than 3 months

- Moderate/severe pain related impairment of everyday activities

Exclusion Criteria:

- Other causes of persistent pain in groin region (hip, other surgical procedures)

- Drug or alcohol abuse

- Conflicting neurological disorders

Study Design

Observational Model: Case-Only


Locations

Country Name City State
Denmark Section of Surgical Pathophysiology, Rigshospitalet, Copenhagen University Copenhagen

Sponsors (2)

Lead Sponsor Collaborator
Rigshospitalet, Denmark Innovative Medicines Initiative

Country where clinical trial is conducted

Denmark, 

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