Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
500 participants
OBSERVATIONAL
2019-10-07
2020-08-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Chronic postoperative pain
Patients scoring 3 or more on the EuraHS Quality of Life assessment after elective inguinal hernia repair
Inguinal hernia repair
Inguinal hernia repair (open, laparo-endoscopic, robotic)
Non chronic postoperative pain
Patients scoring less than 3 on the EuraHS Quality of Life assessment after elective inguinal hernia repair
Inguinal hernia repair
Inguinal hernia repair (open, laparo-endoscopic, robotic)
Interventions
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Inguinal hernia repair
Inguinal hernia repair (open, laparo-endoscopic, robotic)
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Willing and able to consent and comply with the follow up protocol
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University of Lisbon
OTHER
Portuguese Surgical Research Collaborative
NETWORK
Responsible Party
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Principal Investigators
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Antonio Soares
Role: STUDY_CHAIR
Portuguese Surgical Research Collaborative
Locations
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Hospital prof. Dr. Fernando Fonseca
Lisbon, , Portugal
Countries
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Other Identifiers
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Version 1
Identifier Type: -
Identifier Source: org_study_id
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