Clinical study of inguinal hernia mesh fixation with fibrin glue

Clinical study on fixation of inguinal hernia mesh with fibrin glue

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-jRCT1071230076

Enrollment

Registered

2023-10-17

Start date

2023-10-05

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 hernia

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: (1) Patients undergoing hernia repair by TEP who wish to undergo hernia mesh fixation using fibrin glue. (2) Patients who are at least 20 years of age at the time of consent (3) Patients who fully understand this research plan and can give written consent.

Exclusion criteria

Exclusion criteria: (1) Patients with a history of hypersensitivity to components of fibrin glue or drugs made from bovine lung (e.g. aprotinin) (due to contraindication to fibrin glue) (2) Patients undergoing treatment with coagulation accelerators (snake venom preparations) or antifibrinolytic agents (because of contraindications to the use of fibrin glue) (3) Other patients whom the investigator deems inappropriate as research subjects.

Design outcomes

Primary

Measure	Time frame
Early recurrence (recurrence within 3 months after surgery)	—

Secondary

Measure	Time frame
Postoperative pain (VAS), hematoma/seroma development, mesh fixation time	—

Contacts

Public ContactHiroki TOMA

HARASANSHIN Hospital

toma@surg1.med.kyushu-u.ac.jp+81-92-291-3434

Outcome results