N/A N=34 Treatment

Mesh Fixation and Closure of Peritoneum Following Laparoscopic Hernia Repair Using N-butyl Cyanoacrylate

Hernia, Inguinal

Bottom Line

View on ClinicalTrials.gov: NCT02457728 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Dec 2015

Primary outcome: Primary: Number of Participants With Safe Fixation of Mesh and Closure of Peritoneum by Clinical Investigation During Hospital Stay and Telephone Interview at Six Weeks Postoperatively. — 6 participants

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: LiquiBandFix8 (Device)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: St John of God Hospital, Vienna
Primary completion: Aug 2015

Outcome Measures

Outcome	Result	p-value
PRIMARY Number of Participants With Safe Fixation of Mesh and Closure of Peritoneum by Clinical Investigation During Hospital Stay and Telephone Interview at Six Weeks Postoperatively.	6	—

Summary

Fixation of mesh and peritoneal closure during TAPP repair using n-butyl cyanoacrylate.

Eligibility Criteria

Inclusion Criteria

Inguinal hernia,
femoral hernia

Exclusion Criteria

pregnancy,
not able to understand patient information

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02457728). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.