An Observational Study of Recurrence of Inguinal Hernia After Repair Using Parietex Lap-Progrip

An Observational Study of Recurrence of Inguinal Hernia After Repair Using Parietex Lap-Progrip - An Observational Study of Recurrence of Inguinal Hernia After Repair Using Parietex Lap-Progrip

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000020097

Enrollment

Registered

2015-12-07

Start date

2015-12-11

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

inguinal herunia

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)20 years old or older 2)Written informed consent for study participation has been obtained from the patient. 3)Patients who can be followed for 24 months or more postoperatively.

Exclusion criteria

Exclusion criteria: 1)Recurrent inguinal hernia 2)Emergency surgery 3)Patients with incarcerated hernia 4)Other patients judged by the investigator to be inappropriate to participate in this study

Design outcomes

Primary

Measure	Time frame
Hernia recurrence rate within 2 year following the procedure	—

Secondary

Measure	Time frame
1)Postoperative pain (Numeric Rating Scale) 2)Adverse events (bleeding, selome, hematoma, infection, edema, allergic reaction to the products structural materials, intestinal obstruction, and urinary retention due to anesthesia) 3)Patient satisfaction level 4)Operative time 5)Length of hospital stay 6)No of Parietex Lap-Progrip used, cost 7)Whether trimming is required or not	—

Countries

Japan

Contacts

Public ContactMasakazu Ouchi

Juntendo University Urayasu Hospital Surgical Department

ouchimasakazu@yahoo.co.jp047-353-3111

Outcome results