Prospective observational study with mesh fixation using FDA approved synthetic glue,glubran 2 and standard mesh fixation with stiches in primary inguinal hernia repair surgery. The investigators aim is to recruit 150 patients for the study. The outcomes The investigators would like to determine are : postoperative pain,recurrences and complication rates such as seromas.
Prospective observational study with mesh fixation using FDA approved synthetic glue,glubran 2 and standard mesh fixation with stiches in primary inguinal hernia repair surgery. The investigators aim is to recruit 150 patients for the study. The outcomes The investigators would like to determine are : postoperative pain,recurrences and complication rates such as seromas.
Study Type
OBSERVATIONAL
Enrollment
150
Rambam Health Care Campus
Haifa, Israel
RECRUITINGPostoperative pain (Evaluation will be conducted through scale and a questionnaire )
Time frame: 2 years
Hernia recurrence (Evaluation will be conducted through a questionnaire and physical examination )
Time frame: 2 years
Postoperative complications (Evaluation will be conducted through a questionnaire and physical examination )
Time frame: 2 years
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