Factors Influencing the Results of Treatment in Patients With Hernias of Various Localizations
Recruiting
Observational Study
Inguinal Hernia
Femoral Hernia
Umbilical Hernia
Ventral Hernia
Chronic Pain
Acute Post Operative Pain
Recrrence Rate
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 90
- Sex
- Any
- Study type
- Observational
- Participants needed
- 4,000 (estimated)
- Sponsor
- Immanuel Kant Baltic Federal University · Other
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About This Trial
The study attempts to quantify the relative risks for acute postoperative pain, complications rate, chronic postoperative pain (CPIP) and recurrence rate after different methods of repair of groin, umbilical and incisional hernia depending on surgical technique, mesh type and fixation suture material. For this purpose the investigators will analyze data from the Kalinigrad Hernia Registry (KHR).
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* All mesh and non-mesh repairs that have been registered in the KHR from January 9, 2020, until December 31, 2023.
Exclusion Criteria:
* Patients not having a 11-digit state-assigned Personal insurance policy number.
* Parastomal hernia;
* infected hernias;
Contacts