Comparison of Mesh Fixation Wit Cyanoacrylate vs Suture in Inguinal Hernia Surgery

NCT ID: NCT02197585

Last Updated: 2014-07-22

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-06-30

Study Completion Date

2011-06-30

Brief Summary

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To compare fixation with glubran2 with suture during surgery por primary inguinal hernia.

Hypothesis: Glue may induce less complications and chronic pain than suture

Detailed Description

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Conditions

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Chronic Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Glue

Mesh fixation with glue

Group Type EXPERIMENTAL

Inguinal mesh hernioplasty

Intervention Type PROCEDURE

Suture

Mesh fixation with suture

Group Type ACTIVE_COMPARATOR

Inguinal mesh hernioplasty

Intervention Type PROCEDURE

Interventions

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Inguinal mesh hernioplasty

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Male patients
* Aged more than 18 years
* Primary inguinal hernia

Exclusion Criteria

* Inguinoscrotal hernia
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Hospital del Mar

OTHER

Sponsor Role lead

Responsible Party

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José A. Pereira

Medico Adjunto Cirugia General

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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JA Pereira, MD

Role: PRINCIPAL_INVESTIGATOR

Hospital del Mar

Other Identifiers

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UHU

Identifier Type: -

Identifier Source: org_study_id

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