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Inguinal HerniaNCT02424604

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

An observational study of Inguinal Hernia, run by Karolinska Institutet at 1 site in Sweden.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Inguinal Hernia
How many people
2,000 participants
Where
1 siteSweden
Study dates
Apr 2015to Dec 2016
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: patinets with relapse after inguinal hernia surgery

Who may be able to join

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

Who cannot join

  • none

Trial locations and contacts

1 site in 1 country.

Sweden1 site
  • Ersta Hospital

    Stockholm, 116 91

Other trials in Sweden

About this study

Official title: Recurrency After Inguinal Herniorraphy With Bi-layer Mesh

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

Read the detailed description

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.

Conditions
Inguinal Hernia
Medical subject headings
Hernia, Inguinal

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of recurrence

    Recurrence rate for BLM in Inguinal hernia surgery

    Measured: up to 30 days after surgery

Secondary outcomes (1)
  1. Number of surgical methods (BML and Lichtenstein)

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

    Measured: up to 30 days after surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Apr 2015 (estimated)
  2. Study startApr 2015
  3. Primary completionDec 2016
  4. Study completionDec 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
2,000 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02424604
Sponsor's protocol ID
EPN 2015/351-31/1
Status last verified
Mar 2016
First submitted
7 Apr 2015
Last updated
13 Mar 2017
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Inguinal Hernia, run by Karolinska Institutet at 1 site in Sweden.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Mar 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of recurrence (time frame: up to 30 days after surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Mar 2017.

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