Skip to content

3-point With 1-point Mesh Fixation in TAPP for Inguinal Hernia

A Comparative Study of 3-point With 1-point Mesh Fixation in TAPP for Inguinal Hernia

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06314152
Enrollment
351
Registered
2024-03-15
Start date
2023-01-01
Completion date
2025-10-10
Last updated
2026-04-09

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

Conditions

Chronic Pain, Hematoma, Infections, Inguinal Hernia, Recurrent, Seroma

Brief summary

This study was designed to compare the outcome of 3 point with 1 point lightweight mesh fixation in TAPP surgery for patients with inguinal hernia. The main outcome include seroma, chronic pain, recurrence, et al.

Interventions

PROCEDURELightweight mesh fixation in 3 points or 1 point

Lightweight mesh fixation in 3 points

Sponsors

Nanchong Central Hospital
Lead SponsorOTHER_GOV
Guang'an People's Hospital
CollaboratorUNKNOWN
Pengan County People's Hospital
CollaboratorOTHER
People's Hospital of Yilong County
CollaboratorUNKNOWN
Nanbu Hospital of County Chinese Medicine
CollaboratorOTHER
Langzhong People's Hospital
CollaboratorUNKNOWN
Langzhong Traditional Chinese Medicine Hospital
CollaboratorUNKNOWN

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Unilateral inguinal hernia according to preoperative physical examination and imaging examination. The inclusion criteria were as follows: primary inguinal hernia.

Exclusion criteria

* Age below 18 years or older than 80. recurrent hernia, incarcerated hernia, strangulated hernia, and other types of hernias. Patients not suitable for general anesthesia. Patients requiring open surgery; patients requiring emergency surgery Loss to follow-up or communication difficulties, or poor compliance.

Design outcomes

Primary

MeasureTime frameDescription
Rate of postoperative pain12 monthsThe visual analog scale (VAS) was adopted for pain evaluation 1 day, 7 days, 1 month, 3 months, 6 months and 12 months postoperatively. The scale range from 0 to 10, with 0 meaning no pain and 10 meaning the worst pain.
Rate of recurrence1 month,3 months,6 months and 12 months after surgeryHernia recurrenceFollow up by physical examination, ultrasonography and telephone at 1 month,3 months,6 months and 12 months after surgery about the rate of hernia recurrence.

Secondary

MeasureTime frameDescription
Rate of postoperative complications12 monthsIncluding infection, seroma, hematoma

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 10, 2026