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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02632097
Acronym
Histoacryl1
Enrollment
370
Registered
2015-12-16
Start date
2013-03-31
Completion date
2017-01-31
Last updated
2017-03-03

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

Conditions

Inguinal Hernia

Keywords

inguinal hernia, mesh fixation, glue, cyanoacrylate, Lichtenstein, ambulatory surgery

Brief summary

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.

Detailed description

Hypothesis: 1. To use glue (instead of sutures) for mesh fixation during open hernioplasty causes a lower immediate postoperative pain. 2. The use of Histoacryl is associated to a lower postoperative complications rate. 3. 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.

Interventions

PROCEDURELichtenstein Hernioplasty with Histoacryl

Procedure/Surgery: Lichtenstein Hernioplasty with Histoacryl: 0.5 ml of cyanoacrylate glue is used for mesh fixation

PROCEDURELichtenstein Hernioplasty with Sutures

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

Sponsors

Hospital Plató
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Acute Postoperative Pain30 dayspain scores (VAS 0-10) after surgery
Operating Time30 daysoperating time needed to perform hernioplasty

Secondary

MeasureTime frameDescription
Postoperative Complications30 daysComplications related to procedure and assessed according to Clavien-Dindo Classification
Early Recurrence Rate1 yearInguinal hernia recurrence rate after 1 year follow-up
Chronic Pain1 yearPain scores (0-10) after 1-year follow-up
Late Recurrence Rate5 yearsInguinal hernia recurrence rate after 5 years follow-up

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026