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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

18-75 Years
18+ Years
All
All

Not accepting

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?

Yes

Inclusion Criteria

- Patients with surgical indication for hemorrhoids, fistula-in-ano or anal fissures.

- Age of 18 or above

No

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

Locations

Location

Status