Evaluation of short-term outcomes of robot-assisted inguinal hernia repair for primary groin hernia patients -Multicenter, Prospective cohort study
Not Applicable
- Conditions
- inguinal hernia
- Registration Number
- JPRN-UMIN000046048
- Lead Sponsor
- Teikyo University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 109
Inclusion Criteria
Not provided
Exclusion Criteria
1)ASA-PS is Class 3 or higher 2)Patients undergoing emergency surgery 3)Patients with incarcerated hernia 4)Patients undergoing surgery for recurrence (including recurrence after childhood hernia treatment) or postoperative pain 5)Patients with a history of lower abdominal surgery (including urologic/gynecologic surgery) or laparotomy (not excluding contralateral inguinal hernia surgery) 6)Patients who are unable to self-evaluation pain (e.g., dementia, psychiatric disorders) 7)Pregnant patient 8)Other patients who are deemed inappropriate by the investigator as subjects of the study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intraoperative adverse events
- Secondary Outcome Measures
Name Time Method