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CompletedNCT05378451TOHERUpdated Mar 20, 2024

Totally Extraperitoneal Repair of Groin Hernia in Liver Transplanted Patients

An observational study in Liver Transplant Disorder, Liver Cirrhosis and Groin Hernia, sponsored by Hospital Clinic of Barcelona. Completed at 1 site in Spain. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-03-20.

Sponsored by Hospital Clinic of Barcelona · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
10
Ages
18 Years and older
Sex
All
01

Study summary

Liver transplant recipients share the risk with cirrhotic patients for the development of inguinal hernias, but their liver failure pathophysiology has reversed following transplantation. Despite immunosuppression alters wound healing and infections, inguinal hernia repair in transplanted patients has shown better outcome compared to cirrhotic patients. Endoscopic inguinal hernia techniques have proved to be superior to open repair, due to lower incidence of postoperative complications and short-term convalescence, but there is no evidence of the use of this approach in liver transplanted patients. This prospective consecutive case series study will be the first study to describe the postoperative results of groin hernia repair in ambulatory surgery regimen in liver transplanted patients using totally extraperitoneal approach. The included patients will be prospectively registered in a standardized database. Rate of completion of surgery by totally extraperitoneal approach without the needing of conversion to anterior open approach or transabdominal preperitoneal approach due technical difficulties will be evaluated. Postoperative complications all along with quality standards criteria of ambulatory surgery will be reported for descriptive purposes.

Read the detailed description

This will be a single center prospective consecutive case series study. Liver transplanted patients diagnosed of groin hernia will be operated using endoscopic totally extraperitoneal approach in ambulatory surgery regimen. Main objective will be to evaluate the rate of completion of surgery by totally extraperitoneal approach without the needing of conversion to anterior open approach or transabdominal preperitoneal approach due technical difficulties. Secondary objectives will be to record postoperative complications all along with quality standards criteria of ambulatory surgery.

The sample size could not be formally calculated as this is a pilot study. It is the first time that the surgical team has considered this type of surgical approach and we wish to evaluate the feasibility of this technique. Since in our center the number of surgical procedures of groin hernia in liver transplanted patients could be around 20 per year, for this pilot study we propose recruiting between 15-20 patients. The results will be representative of this type of surgical activities in a tertiary university hospital.

Liver transplanted patients diagnosed with groin hernia planned to undergo ambulatory surgical repair will be considered for being included in the study after informed consent. Perioperative management will be provided as determined by the local clinical practice without modifications due to study inclusion.The included patients will be prospectively registered in a standardized database. Background information and details regarding the surgery will be retrieved from the patients' medical records.

Information regarding postoperative complications will be collected up to 30 days after surgery. Following routine clinical practice, including telephonic contact on first postoperative 24h, clinical control follow up at 10 days and at month after the surgery.

This case series has been reported in line with the PROCESS Guideline.

02

Conditions studied

  • Liver Transplant Disorder
  • Liver Cirrhosis
  • Groin Hernia

Keywords

  • Liver Trasplant
  • Groin Hernia
  • Totally Extraperitoneal Repair
03

In context

Liver Cirrhosis

1,642 studies on the registry are indexed under Liver Cirrhosis; 358 are open to participants now.

This study's enrollment of 10 is below the median of 151 across 587 observational studies indexed under Liver Cirrhosis.

Browse Liver Cirrhosis studies →

Lead sponsor

Hospital Clinic of Barcelona is the lead sponsor of 319 studies on the registry; 55 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Liver transplanted patients diagnosed with groin hernia planned to undergo ambulatory surgical repair will be considered for being included in the study after informed consent. Perioperative management will be provided as determined by the local clinical practice without modifications due to study inclusion.

Inclusion criteria

  • Patients older than 18 years of age.
  • Liver transplanted patients diagnosed from groin hernia and proposed for ambulatory surgery.
  • Signed informed consent for inclusion in the study

Exclusion criteria

Exclusion Criteria:

  • Patients under 18 years of age.
  • Pregnancy or breastfeeding.
  • Inability to give informed consent.
  • Patients not candidates for surgical treatment.
  • Contraindication to general anesthesia.
  • Procedures performed in an emergency setting.
  • Patients non tributary to ambulatory surgery due to anesthesia management (ASA>III or decompensation in the last 3 months)
  • Impossibility for the care of a responsible adult during first 24 hours after surgery.
  • Domicile at a distance of more than 1 hour by vehicle from the hospital.
  • Previous posterior approach for hernia repair.
  • Previous cystectomy and prostatectomy surgery.
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
10 participants (actual)
Patient registry
No

Interventions

  • ProcedureTotally Extraperitoneal Groin Hernia Repair

    Patients will undergo totally extraperitoneal groin hernia repair, by a single senior experimented surgeon and without modifications from the routine clinical practice due to study inclusion. TEP approach will be assessed by placement of 3 trocars in the lower midline. Preperitoneal space will be dissected under direct vision using Spacemaker Dissection Balloon (Applied Medical®). Systematic complete dissection of the myopectineal orifice, Retzius and Bogros spaces will be performed to identify all potential sites of hernia formation. It will be used a laparoscopic self-fixating mesh (ProGrip™). Preperitoneal instillation of local anesthesia (15 mL of 0.5% bupivacaine) will be placed placed by the surgeon under direct visualization into "triangle of pain". Local anesthesia (levobupivacaine 10mL 1%) will be applied in all the incisions.

    Also known as: TEP

06

What researchers measure

Primary outcomes

  1. Rate of completion of surgery by totally extraperitoneal approach

    Rate of completion of surgery by totally extraperitoneal approach without the needing of conversion to anterior open approach or transabdominal preperitoneal approach due technical difficulties.

    Time frame: 0 days (intraoperative)

Secondary outcomes

  1. Rate of intraoperative complications

    Register intraoperative complications (intestinal lesions, urinary bladder lesions, major vascular lesions...)

    Time frame: 0 days (intraoperative)

  2. Rate of postoperative complications

    Register postoperative complications (acute urinary retention, urinary infection, hematoma, seroma, surgical wound infection...)

    Time frame: 30 days (postoperative)

  3. Pain measurement

    Control of pain assessed by Visual Analogue Score (at time of discharge, first postoperative day and after 10 days of surgery).

    Time frame: 10 days (postoperative).

07

Study locations

1 site
  • Hospital Clinic of Barcelona
    Barcelona, 08036, Spain
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Icf, Csr

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 20, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05378451
Lead sponsor
Hospital Clinic of Barcelona
Responsible party
Sponsor
First posted
May 18, 2022
Start date
May 8, 2022
Primary completion
Dec 1, 2023
Completion
Jan 1, 2024
Last update
Mar 20, 2024

Study contacts

Paula Dominguez-Garijo, MD
principal investigator · General Surgery, ICMDM, Hospital Clínic de Barcelona.

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2022. You cannot join it, but the record below documents what was studied.

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