Case Report in Complications After Laparoscopic Transabdominal Preperitoneal Groin Hernia Repair Using LiquiBandFIX8®

Groin Hernia Clinical Trial

Official title:

Laparoscopic Transabdominal Preperitoneal (TAPP) Groin Hernia Repair Using N-butyl-2-cyanoacrylate (LiquiBandFIX8®)for Mesh Fixation and Peritoneal Closure: Case Report About Extraperitoneal Hematoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05952791
• Other study ID #: KeplerUH
• Status: Completed
• Start date: January 5, 2022
• Est. completion date: January 5, 2022

Study information

• Verified date: July 2023
• Source: Kepler University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This an a case report about management and proving the strenght and resistance of LiquiBandFIX8® using for peritoneal closure in a laparoscopic transabdominal preperitoneal groin hernia repair. The patient had anticoagulation due to a mechanical valvula and postoperatively the patient developed a huge hematoma extraperitoneally. Relaparoscopy war performed to identify the problem and check the peritoneal closure.

Description:

This an a case report for proving the strenght and resistance of LiquiBandFIX8® using for peritoneal closure in a laparoscopic transabdominal preperitoneal groin hernia repair (TAPP). The patient had anticoagulation due to a mechanical valvula and postoperatively after TAPP the patient developed a huge hematoma extraperitoneally. The investigatorsperformed relaparoscopy for diagnostic and therapeutic reasons to check stop the bleeding and control the integrety of the peritoneal closure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1
• Est. completion date: January 5, 2022
• Est. primary completion date: January 5, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Retrospective case report of one patient undergoing laparoscopic groin hernia repair

Exclusion criteria:

• not applicable (retrospective)

Related Conditions & MeSH terms

• Groin Hernia
• Hernia
• Hernia, Inguinal

Intervention

Other:
• Surgery
Laparoscopic transabdominal preperitoneal (TAPP) groin hernia repair

Locations

Country	Name	City	State
Austria	Kepler University Hospital	Linz	Upper Austria

Sponsors (1)

Lead Sponsor	Collaborator
Kepler University Hospital

Country where clinical trial is conducted

Austria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Strongness of LiquiBandFIX8®	Mesh dislocation, mesh damage (yes/no)	2 weeks
Primary	Hemtoma	intraperitoneal blood (yes/no)	2 weeks
Primary	Strongness of LiquiBandFIX8®	peritoneal leakage, peritoneal damage (yes/no)	2 weeks