Phase
Condition
Hernia
Treatment
Physiotherapy
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- At the University Hospital of Bern, Kantonsspital Solothurn and Olten and BundeswehrZentralkrankenhaus Koblenz:
Informed Consent as documented by signature (Appendix Informed Consent Form)
Age > 18 years
Capable of judgment
Undergoing elective or emergency abdominal surgery
Laparoscopic or open surgery, midline or transverse incision
- At the University Hospital of Lausanne:
Informed Consent as documented by signature (Appendix Informed Consent Form)
Age > 18 years
Capable of judgment
Undergoing elective open abdominal surgery
Midline or transverse incision
Exclusion criteria (in all four participating centres):
Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders (chronic depression, under antidepressants or neuroleptics), dementia, etc. of the participant
Enrolment of the investigator, his/her family members, employees and other dependent persons
Neuromuscular diseases (such as myasthenia gravis or wheelchair-bound patient)
Preexisting chronic pain disorder, patients under chronic opioid therapy (WHO II and III) or pain modulating drugs (antidepressive medication or antiepileptic medication)
End-stage disease
Patients with preexisting abdominal wall mesh, with the exception of inguinal mesh (after inguinal hernia repair)
Study Design
Study Description
Connect with a study center
BundeswehrZentralkrankenhaus
Koblenz, 56070
GermanyActive - Recruiting
Kantonsspital Olten
Olten, Solothurn 4600
SwitzerlandTerminated
University Hospital of Bern, Inselspital
Bern, 3010
SwitzerlandActive - Recruiting
CHUV, University Hospital of Lausanne
Lausanne, 1010
SwitzerlandActive - Recruiting
Bürgerspital Solothurn
Solothurn, 4500
SwitzerlandSite Not Available
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