Mesh Fixation With a Synthetic Glue in Primary Inguinal Hernia Repair

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02507830

Enrollment

150

Registered

2015-07-24

Start date

2015-08-31

Completion date

2017-07-31

Last updated

2016-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inguinal Hernia

Brief summary

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.

Detailed description

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Primary Inguinal hernia

Exclusion criteria

* Recurrent hernia * Large inguinoscrotal hernias * Bilateral inguinal hernias

Design outcomes

Primary

Measure	Time frame
Postoperative pain (Evaluation will be conducted through scale and a questionnaire )	2 years

Secondary

Measure	Time frame
Hernia recurrence (Evaluation will be conducted through a questionnaire and physical examination )	2 years
Postoperative complications (Evaluation will be conducted through a questionnaire and physical examination )	2 years

Countries

Israel

Contacts

Primary ContactAdel Abu_Salih, MD

a_abu_salih@rambam.health.gov.il972-4-8541308

Outcome results