COMPARISON OF LAPAROSCOPIC TOTAL EXTRAPERITONEAL HERNIA REPAIR AND LICHTENSTEIN HERNIA REPAIR

Inguinal Hernia Clinical Trial

— HERNIA  

Official title:

COMPARISON OF LAPAROSCOPIC TOTAL EXTRAPERITONEAL HERNIA REPAIR AND LICHTENSTEIN HERNIA REPAIR FOR SEXUAL, SENSORY, LIFE QUALITY AND URINARY FUNCTIONS

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03935503
• Other study ID #: ANIL ERGIN1
• Status: Completed
• Start date: July 1, 2017
• Est. completion date: April 1, 2019

Study information

• Verified date: May 2019
• Source: Fatih Sultan Mehmet Training and Research Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

The superiority of laparoscopic inguinal hernia surgery over open surgery has been shown in many high patient-numbered studies with early return to work, less pain and good cosmetic results. The aim of this study is to determine the differences between two different methods in terms of sexual, sensory, quality of life and urinary results.

Description:

Between July 2017 and January 2018, 42 sexually active male patients were randomized with Laparoscopic Total Extraperitoneal (TEP) method and Lichtenstein (LCH) method and repair of inguinal hernia. Patients were evaluated preoperatively, at 1 month and 6 months postoperatively, International Sexual Function Index (IFIF), International Prostatic Symptom Score, SF-36 Quality of Life Scale, Visual Analog Pain Scale, Beck Depression Scale, Inguinal Region Discrimination Test ( DT), DN4 Neuropathic Pain Survey, Uroflowmetry and FSH, LH, Total Testosterone levels were evaluated.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: April 1, 2019
• Est. primary completion date: January 1, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Unilateral inguinal hernia (diagnosed by physical examination or imaging)

• Sexual Active

• Male gender

• aged between 18 and 65

• ASA 1-2

• EHS Classification (Primary, lateral or medial, 1 and 2)

Exclusion Criteria:

• Patients with previous abdominal and inguinal hernia surgery

• ASA 3-4

• Sexually inactive

• Emergency patients (Etrangule inguinal hernia)

Related Conditions & MeSH terms

• Hernia
• Hernia, Inguinal
• Inguinal Hernia

Intervention

Procedure:
• TEP
By making a 2 cm incision under the umbilicus, skin subcutaneous tissues are passed through blunt dissections and the anterior fascia of the rectus muscle is exposed. An anterior rectus sheath with a scalpel is performed with a 15 mm incision. The rectus muscle is laterally lateralized and the balloon trocar or laparoscope itself is advanced from the midline to the symphysis pubis via the posterior rectus sheath. After the peritoneal cavity is dissected, a low pressure pneumoperitone 10 mm Hasson trocar or another 10 mm balloon caged trocar is advanced through the subumblic incision. 9-11 mmHg low pressure pneumoperitoneum is created to prevent the development of subcutaneous emphysema. For proper imaging, the patient should have complete muscle relaxation. The patient is given a position towards the light trandelenburg and non-hernia side.
• Lichtenstein repair
After the inguinal incision, the skin and subcutaneous camper and scarpa tissues are passed and the external oblique aponeurosis is dissected in the direction of the extension of the fibers and the medial lateral edge of the rectus is dissected to the lateral inguinal ligament, then the spermatic cord is released and suspended.The spermatic cord is separated from the inguinal canal. In indirect hernias, the hernia sac is dissected from the spermatic cord and rejected into the abdomen by high ligation. In direct hernia, the hernia sac is pushed in and the transverse fascia is sutured with 2-3 separe stitches.

Locations

Country	Name	City	State
Turkey	Fatih Sultan Mehmet Research and Training Hospital	Istanbul

Sponsors (1)

Lead Sponsor	Collaborator
Fatih Sultan Mehmet Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	International Sexual Function Index (IFIF)	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively.Total 15 questions are included.Answers are include 1-5 options. (1:never , 5:always) Question 1,2,3,4,5,15 for erectile function , Question 9,10 for orgasm function , Question 11,12 for sexual desire , Question 6,7,8 for sexual satisfaction , Question 13,14 for general satisfaction.	UP TO 6 MONTHS
Primary	International Prostatic Symptom Score	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively. Total 7 questions which are about urinary functions are included.Answers are include 1-5 options. (1:never , 5:always) . Questions are : what is your frequency of feeling that your bladder does not empty after urination; what is the frequency of needing to urinate in less than 2 hours after urination?; what is your frequency of stopping several times when you urinate and restart?; how often do you have difficulty urinating?; how often did you feel the reduction in the power of your urine?; how often have you experienced difficulty urinating?; how many times have you gone to urinate until you get up in the morning?	UP TO 6 MONTHS
Primary	SF-36 Quality of Life Scale	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively	UP TO 6 MONTHS
Primary	Visual Analog Pain Scale	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively.pain scores (VAS: from 0 to 10, 0 = no pain, 10 = the worst pain) The higher score idicates the worse outcome.	UP TO 6 MONTHS
Primary	Beck Depression Scale	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively	UP TO 6 MONTHS
Primary	Inguinal Region Discrimination Test ( DT)	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively	UP TO 6 MONTHS
Primary	DN4 Neuropathic Pain Survey	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively. There are 4 questions in this survey and includes totally 10 points in it. Above the 4 points mean it is a neuropathic pain.	UP TO 6 MONTHS
Primary	Uroflowmetry test for urination	In our study, the evaluation of urinary functions was performed with urolowmetry. Patients were evaluated preoperatively, at 1 month and 6 months postoperatively Voiding flow rates and voiding volumes were compared before and after surgery with Uroflowmetry	UP TO 6 MONTHS
Primary	Follicle Stimulating Hormone levels	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively	UP TO 6 MONTHS
Primary	Luteinising Hormone levels	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively	UP TO 6 MONTHS
Primary	Total Testosterone levels	Patients were evaluated preoperatively, at 1 month and 6 months postoperatively	UP TO 6 MONTHS