Perioperative monitoring of inguinal hernia patients with a smartphone application, a pilot study
Completed
- Conditions
- Inguinal hernia
- Registration Number
- NL-OMON22945
- Lead Sponsor
- na
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 250
Inclusion Criteria
Primairy inguinal hernia, adult, Dutch language, no cognitive impairment, in possession of smartphone or tablet with Android or iOS operating system
Exclusion Criteria
Previous inguinal (hernia) surgery, < 18 yr, insufficient language (Dutch) skills, cognitive impairment
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method CPIP (chronic postoperative inguinal pain) 3 months post operative
- Secondary Outcome Measures
Name Time Method Surgical site infection, return to work / daily activities