Clinical study of inguinal hernia mesh fixation with fibrin glue
Not Applicable
Recruiting
- Conditions
- inguinal hernia
- Registration Number
- JPRN-jRCT1071230076
- Lead Sponsor
- TOMA Hiroki
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 20
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
(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.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Early recurrence (recurrence within 3 months after surgery)
- Secondary Outcome Measures
Name Time Method Postoperative pain (VAS), hematoma/seroma development, mesh fixation time