Perianal Nerval Block in Proctological Interventions
Sponsored by University Hospital, Basel, Switzerland
About this trial
Last updated 6 years ago
Study ID
Perianal block in proctology
Status
Completed
Type
Interventional
Phase
Phase 4
Placebo
No
Accepting
18+ Years
All
Not accepting
Healthy Volunteers
Trial Timing
Ended 6 years ago
What is this trial about?
The aim of this study is to evaluate whether a local perianal block performed during a
proctological intervention can reduce the postoperative pain.
What are the participation requirements?
Inclusion Criteria
- Patients with surgical indication for hemorrhoids, fistula-in-ano or anal fissures.
- Age of 18 or above
Exclusion Criteria
- age under 18.
- Patients unable to understand an informed consent.
- Emergency operations
- Pregnant women.
- Patients with acute perianal infection.
- Patients allergic to any component of the local anesthetic