NCT05952791

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jan 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 5, 2022

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 5, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 5, 2022

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

June 7, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 19, 2023

Completed
Last Updated

July 19, 2023

Status Verified

July 1, 2023

Enrollment Period

Same day

First QC Date

June 7, 2023

Last Update Submit

July 17, 2023

Conditions

Groin Hernia

Outcome Measures

Primary Outcomes (3)

  • Strongness of LiquiBandFIX8®

    Mesh dislocation, mesh damage (yes/no)

    2 weeks

  • Hemtoma

    intraperitoneal blood (yes/no)

    2 weeks

  • Strongness of LiquiBandFIX8®

    peritoneal leakage, peritoneal damage (yes/no)

    2 weeks

Interventions

SurgeryOTHER

Laparoscopic transabdominal preperitoneal (TAPP) groin hernia repair

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Retrospective case report of one patient

You may qualify if:

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

You may not qualify if:

  • \- not applicable (retrospective)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kepler University Hospital

Linz, Upper Austria, 4020, Austria

Location

MeSH Terms

Conditions

Hernia, Inguinal

Interventions

Surgical Procedures, Operative

Condition Hierarchy (Ancestors)

Hernia, AbdominalHerniaPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Study Officials

  • Sandra Raab, MD

    Kepler University Hospital Linz

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 7, 2023

First Posted

July 19, 2023

Study Start

January 5, 2022

Primary Completion

January 5, 2022

Study Completion

January 5, 2022

Last Updated

July 19, 2023

Record last verified: 2023-07

Data Sharing

IPD Sharing
Will not share

Locations

AU(1)