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Perianal Nerval Block in Proctological Interventions

NCT03405922 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 166

Last updated 2019-07-10

No results posted yet for this study

Summary

The aim of this study is to evaluate whether a local perianal block performed during a proctological intervention can reduce the postoperative pain.

Conditions

Interventions

DRUG

Placebo 40 mL Saline 0.9%

Injection of 40 mL 0.9% saline

DRUG

40 mL Ropivacain 0.5%

Ropivacaine Hcl 0.5% Injection 40 mL

Sponsors & Collaborators

  • University Hospital, Basel, Switzerland

    lead OTHER

Principal Investigators

  • Daniel Steinemann · St:Claraspital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-01
Primary Completion
2019-07-05
Completion
2019-07-05

Countries

  • Switzerland

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03405922 on ClinicalTrials.gov