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OpenTrials
Completed

NCT Number: NCT02632097

Histoacryl™ vs. Suture for Mesh Fixation in Lichtenstein Hernioplasty: A Randomized Prospective Double-Blinded Study

This is a prospective, randomized double-blinded study to find out if mesh fixation with n-butyl-2-cyanoacrylate (NBCA) are more painless than conventional mesh fixation with sutures in inguinal hernia operation (Lichtenstein procedure) in day-case surgery. Our hypothesis is that glue fixation is safe, simple and fast method compared to conventional Lichtenstein technique.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Plató

Barcelona, 08006, Spain

About this study

Hypothesis:

  • To use glue (instead of sutures) for mesh fixation during open hernioplasty causes a lower immediate postoperative pain.
  • The use of Histoacryl is associated to a lower postoperative complications rate.
  • The use of Histoacryl is not associated to a higher hernia recurrence rate.

Methods:

350 patients with inguinal hernia undergone Lichtenstein operation in day-case surgery setting. Mesh fixation is performed using 2 methods: cyanoacrylate glue: Histoacryl™ (n=175: Group H), and non-absorbable sutures: polypropylene 2/0 (n=175: Group S). Operative time and pain scores, immediate postoperative outcome are followed 1, 7, 30 days and 1 and 5 years postoperatively.

Surgeon doesn't know previously which fixation method will be used in each patient. This method (glue or sutures) is decided intraoperatively, when mesh is placed, using a blind randomization code (www.randomizer.org) Patients are discharged (day-case surgery) if adequate pain control, oral tolerance and spontaneous diuresis is achieved, and after examination by the surgeon in order to discard immediate complications. Postoperative oral treatment is prescribed to patients of both groups: dexketoprofen 25 mg/8 h + paracetamol 1 gr/8.

Follow-up is performed at the medical office by a blind observer (third surgeon) who didn't participate in the surgical procedure, at 1 day, 7 days, 30 days, 1 year and annually thereafter. Pain is measured using a VAS scale (0-10).

Operative data (including operating time, complications, hospital stay, etc.), early and late complications, acute and chronic pain and recurrence rate will be recorded.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • unilateral inguinal hernia
  • primary hernia

Exclusion criteria

  • femoral hernia
  • recurrent inguinal hernia
  • immunosuppression (including corticosteroids, radiotherapy, chemotherapy)
  • chronic renal failure (hemodialysis)
  • active infection
  • pregnancy
  • allergy to polypropylene
  • patient's refusal

Treatment and study plan

Lichtenstein Hernioplasty with Histoacryl

Procedure

Procedure/Surgery: Lichtenstein Hernioplasty with Histoacryl:

0.5 ml of cyanoacrylate glue is used for mesh fixation

Lichtenstein Hernioplasty with Sutures

Procedure

Procedure/Surgery: Lichtenstein Hernioplasty with Sutures: non-absorbable suture (polypropylene 2/0) is used for mesh fixation Other Name: prolene 2-0

Primary outcomes

  1. Acute Postoperative Pain

    Time frame: 30 days

    pain scores (VAS 0-10) after surgery

  2. Operating Time

    Time frame: 30 days

    operating time needed to perform hernioplasty

Secondary outcomes

  1. Postoperative Complications

    Time frame: 30 days

    Complications related to procedure and assessed according to Clavien-Dindo Classification

  2. Early Recurrence Rate

    Time frame: 1 year

    Inguinal hernia recurrence rate after 1 year follow-up

  3. Chronic Pain

    Time frame: 1 year

    Pain scores (0-10) after 1-year follow-up

  4. Late Recurrence Rate

    Time frame: 5 years

    Inguinal hernia recurrence rate after 5 years follow-up

Sponsors and collaborators

Lead sponsor

Hospital Plató

Other

Registry information

Official study title

Randomized Prospective Double-Blinded Study of Histoacryl™Mesh Fixation Compared to Conventional Non-absorbable Suture Fixation During Lichtenstein Hernioplasty

Acronym: Histoacryl1

Important dates

Study start
2013
Primary completion
2016
Study completion
2017
First posted
Dec 16, 2015
Registry last updated
Mar 3, 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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