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Laparscopic Hernioplasty in Recurrent Inguinal Hernia

A Prospective Randomized Pilot Study Comparing Transabdominal Properitoneal (TAPP) Versus Totally Extra Peritoneal (TEP) Laparoscopic Inguinal Hernioplasty in Recurrent Inguinal Hernia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06050538
Enrollment
44
Registered
2023-09-22
Start date
2021-02-01
Completion date
2023-08-01
Last updated
2023-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent Inguinal Hernia

Keywords

TAPP, TEP, Laparoscopic Inguinal Hernia, Recurrent hernia

Brief summary

The purpose of this study was to compare between laparoscopic transabdominal preperitoneal (TAPP) and totally extraperitoneal (TEP) repair of inguinal hernia in recurrent inguinal hernia.

Detailed description

The primary objective in this study was to compare postoperative pain between the TAPP group and the TEP group. The secondary objective was to compare operative time, intraoperative complications (bleeding, bowel injury, vascular injury), postoperative complications (hematoma, seroma, wound infection), length of hospital stay and recurrence rate with possible risk factors which include gender, age, BMI ,cord lipomas and location of the hernia.

Interventions

PROCEDURETransabdominal preperitoneal (TAPP) using polyprolene mesh

Transabdominal preperitoneal (TAPP) approach for recurrent inguinal hernia using polyprolene mesh

PROCEDURETotal extraperitoneal (TEP) hernioplasty using polyprolene mesh

Total extraperitoneal (TEP) approach for recurrent inguinal hernia using polyprolene mesh

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Masking description

Each patient was randomly allocated to the TAPP group or the TEP group by sequentially numbered, opaque , sealed envelope (SNOSE) technique on the day of surgery. An independent statistician , who was not involved in patient care, generated the randomization sequence via a computer generated random number. The randomization code was contained in opaque sealed envelopes. A junior resident , who opened the envelope , was not actively involved in outcome measurements .Before randomization and during the consent, all patients received an explanation of the objectives of the study, techniques and complications associated with both procedures.

Intervention model description

patients diagnosed with recurrent inguinal hernia. The study population were randomly distributed into 2 groups by computer generating program; group (1) included patients who had Transabdominal preperitoneal (TAPP) approach while group (2) included patients who had Total extraperitoneal (TEP) approach.

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with unilateral or bilateral recurrent inguinal hernias. * Patients between 18 and 70 years old * Fit for anesthesia. * Agree to participate in the study * Both genders were included.

Exclusion criteria

* Unfitness for general anesthesia and operation. * Age \< 18 years or \>70 years. * Complicated hernias (acute irreducible, obstruction or strangulation). * The presence of mental or psychological disorders. * Refusal to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative pain6 monthsby use of visual analog scale (VAS) where (0) refereed to no pain and (10) refereed to the severest pain.

Secondary

MeasureTime frameDescription
operative time6 monthsoperative time by minutes was reported to get mean and standard deviation
complications6 monthscomplications will be described as number and percentages in each group

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026