Prospective Study Assessing the Laparoscopic Totally ExtraPeritoneal (TEP) Hernia Repair Without Curare and Without Orotracheal Intubation (Free Curare TEP Study).

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

Laparoscopic treatment of inguinal hernia with the totally extraperitoneal approach (TEP) is indicated for simple and bilateral inguinal hernias. It consists of placing a large prosthesis in the posterior position by direct access to the extra-peritoneal space. This prosthesis is interposed between the defective wall and the peritoneum. Unlike the transperitoneal laparoscopic method, the strictly extraperitoneal approach reduces complications related to contact with the intestinal loops and preserves the peritoneal layer intact. TEP approach is traditionally performed under general anesthesia with curare and orotracheal intubation. In the study, we would like to assess this intervention without curare and without standard orotracheal intubation but with a laryngeal mask airway to permit ventilation.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Male or female aged 18 or over

• BMI below 30

• Non-recurrent unilateral hernia

• Operating time estimated at less than 60 minutes at the surgeon's discretion

• Patients eligible to an ambulatory surgical setting at the discretion of the surgeon and the anesthetist

• Patient informed of the study and agreed to take part.

Locations
Other Locations
France
Nouvel Hôpital Privé Les Franciscaines
RECRUITING
Nîmes
Contact Information
Primary
David Amielh, MD
davidamielh@gmail.com
04 66 38 97 67
Time Frame
Start Date: 2022-11-21
Estimated Completion Date: 2024-06
Participants
Target number of participants: 60
Treatments
Hernia repair with laparoscopic TEP approach without curare and without orotracheal intubation.
Patients will undergo laparsocopic TEP hernia repair without curare and without orotracheal intubation.
Related Therapeutic Areas
Sponsors
Leads: Elsan

This content was sourced from clinicaltrials.gov

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