Inguinal hernia
Conditions
Interventions
Experimental group:Wear the new adjustable pressure hernia protection device for 2 weeks
Control group:None
Sponsors
Capital Medical University Affiliated Beijing Chaoyang Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Age >= 18 years; 2. After unilateral primary inguinal hernia repair surgery; 3. Willing and able to complete all study procedures and comply with the entire study process; 4. Willing to sign a written informed consent form.
Exclusion criteria
Exclusion criteria: 1. Recurrent hernia; 2. Bilateral hernia; 3. Undergoing inguinal hernia repair surgery simultaneously with other surgeries; 4. Avascular necrosis of the femoral head, local skin infection, or local skin disease; 5. Use of biological mesh; 6. Intraoperative or postoperative complications of other types, such as hematoma, urinary retention, intestinal injury, mesh infection, postoperative bleeding, severe complications involving major organ dysfunction, etc.; 7. Pregnant or breastfeeding; 8. Currently participating in or having participated in other drug or medical device clinical trials within the past three months prior to enrollment; 9. History of severe organ dysfunction, such as cirrhosis or renal insufficiency; 10. Other circumstances deemed unsuitable for participation in this study by the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of postoperative seroma; | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual analogue scale score;Carolinas Comfort Scale score; | — |
Countries
China
Contacts
Public ContactWang Minggang
Beijing Chaoyang Hospital, Capital Medical University
Outcome results
None listed