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Completed

NCT Number: NCT02424604

Recurrency After Inguinal Herniorraphy With Bi-layer Mesh (BLM)

Aim The overall aim with this study is to improve outcome after inguinal hernia repair (IHR). It is not known today if a re-operation due to recurrence after bi-layer mesh IHR is more complicated than compared with the golden standard method.

Method This project is a registry study. The National hernia register (Svenskt bråckregister, SBR) which started in 1992 include data that cover nearly 100% of all the country's hernia operations.

Patient data are collected from SBR. Patients who at the time of surgery were between 18-75 years of age and operated on due to primary inguinal hernia with any of the two mentioned techniques between 1992-2012 are eligible

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Ersta Hospital

Stockholm, 116 91, Sweden

About this study

Background Surgical repair for inguinal hernia is the most common surgical procedure in the world. Since the introduction of repair with mesh reinforcement, relapses have decreased significantly. Recurrence of inguinal hernia affects only 1-2% after inguinal hernia repair (IHR) [1] and is no longer considered to be a big problem. One problem is that a large proportion of patients undergoing surgery develop chronic pain from the surgical area [2-4]. New meshes, with new design and new materials are continuously being introduced, with the aim of reducing the incidence of chronic pain. One of the most common meshes in use today is the so-called "double-mesh" (bi-layer mesh) [1, 5]. Several studies have shown that bi-layer mesh can lead to some gains for the patient initially after surgery, but there is no scientific evidence available that suggest that bi-layer mesh is superior the traditional tension-free mesh repair in the long term [6, 7]. Several reports have shown that bi-layer mesh repair give results as good as the golden standard method, where a single sheet mesh is used.

The surgical technique differ somewhat with respect to which layer of the abdominal is being used [8], when using a bi-layer- or a single sheet mesh. With the bi-layer mesh you use the abdominal layer that is usually used (the pre-peritoneal space) in case of re-operation due to recurrence after open mesh repair. Re-operation after bi-layer mesh IHR is incompletely studied and it is unclear if this is a more difficult surgical procedure compared with re-operation for recurrence after standard IHR.

Aim The overall aim with this study is to improve outcome after IHR. It is not known today if a re-operation due to recurrence after bi-layer mesh IHR is more complicated than compared with the golden standard method.

Method This project is a registry study. The National hernia register (Svenskt bråckregister, SBR) which started in 1992 include data that cover nearly 100% of all the country's hernia operations.

Patient data are collected from SBR. Patients who at the time of surgery were between 18-75 years of age and operated on due to primary inguinal hernia with any of the two mentioned techniques between 1992-2012 are eligible.

Statistics Parametric and non-parametric statistical methods for descriptive analysis will be used for comparison within and between the groups. Students t-test.

Power calculation The primary outcome variable for this registry study is the prevalence of recurrence after bi-layer mesh IHR. This is incompletely mapped. There is no need of a power calculation because the material of the registry is very large and any relevant differences between the groups should easily be detected.

Gain of knowledge The results of the study could show that either method of IHR (eg bi-layer mesh) is less suitable in surgical repair of inguinal hernia, which could be troublesome for those patients who had surgery with the method.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • all patients in a national registry "inguinal hernia" who had had a relapse after inguinal surgery between 1992-2012

Exclusion criteria

  • none

Treatment and study plan

Primary outcomes

  1. Number of recurrence

    Time frame: up to 30 days after surgery

    Recurrence rate for BLM in Inguinal hernia surgery

Secondary outcomes

  1. Number of surgical methods (BML and Lichtenstein)

    Time frame: up to 30 days after surgery

    Surgical methods used in reoperation due to relapse after BML and Lichtenstein?

Other outcomes

  1. Minutes, time of surgery

    Time frame: up to 30 days after surgery

    Surgery time due to relapse after BML and Lichtenstein

  2. Number of complications

    Time frame: up to 30 days after surgery

    Complication due to relapse, after BML and Lichtenstein?

Sponsors and collaborators

Lead sponsor

Karolinska Institutet

Other

Registry information

Official study title

Recurrency After Inguinal Herniorraphy With Bi-layer Mesh

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Apr 23, 2015
Registry last updated
Mar 13, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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