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

• Sponsor: Kepler University Hospital (Other)
• Overall Status: Completed
• CT.gov ID: NCT05952791
• Collaborator: (none)
• Enrollment: 1
• Location: 1

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Groin Hernia	Other: Surgery

Detailed 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.

Study Design

• Study Type: Observational
• Actual Enrollment: 1 participants
• Observational Model: Case-Only
• Time Perspective: Retrospective
• 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
• Actual Study Start Date: Jan 5, 2022
• Actual Primary Completion Date: Jan 5, 2022
• Actual Study Completion Date: Jan 5, 2022

Outcome Measures

Primary Outcome Measures

1. Strongness of LiquiBandFIX8® [2 weeks]

   Mesh dislocation, mesh damage (yes/no)

2. Hemtoma [2 weeks]

   intraperitoneal blood (yes/no)

3. Strongness of LiquiBandFIX8® [2 weeks]

   peritoneal leakage, peritoneal damage (yes/no)

Eligibility Criteria

Criteria

• Ages Eligible for Study: N/A and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

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

Exclusion criteria:

• not applicable (retrospective)

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Kepler University Hospital	Linz	Upper Austria	Austria	4020

Sponsors and Collaborators

• Kepler University Hospital

Investigators

• Principal Investigator: Sandra Raab, MD, Kepler University Hospital Linz

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Kepler University Hospital
• ClinicalTrials.gov Identifier: NCT05952791
• Other Study ID Numbers: KeplerUH
• First Posted: Jul 19, 2023
• Last Update Posted: Jul 19, 2023
• Last Verified: Jul 1, 2023

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Hernia; Hernia, Inguinal

Study Results

No Results Posted as of Jul 19, 2023