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Portuguese Inguinal Hernia Cohort (PINE) Study

NCT04328597 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2020-04-01

No results posted yet for this study

Summary

Prospective national cohort study of patients submitted to elective inguinal hernia repair. The primary outcome is the prevalence of chronic postoperative inguinal pain, according to the EuraHS QoL questionnaire at 3 months postoperatively. The study will be delivered in all Portuguese regions through a collaborative research network. Four 2-week inclusion periods will be open for recruitment. A site-specific questionnaire will capture procedure volume and logistical facilities for hernia surgery.

Conditions

Interventions

PROCEDURE

Inguinal hernia repair

Inguinal hernia repair (open, laparo-endoscopic, robotic)

Sponsors & Collaborators

  • University of Lisbon

    collaborator OTHER

  • Portuguese Surgical Research Collaborative

    lead NETWORK

Principal Investigators

  • Antonio Soares · Portuguese Surgical Research Collaborative

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-07
Primary Completion
2020-06-12
Completion
2020-08-12

Countries

  • Portugal

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04328597 on ClinicalTrials.gov