MedTrace Logo

Assessment and Prevention of Acute Post-herniotomy Pain

NCT01345162 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2014-06-09

Study results available
· View outcomes & findings →

Summary

The aim of the study is the assessment and management of Acute Post-herniotomy Pain using two different therapeutical protocols per os: ketorolac versus association of acetaminophene+tramadol.

Conditions

  • Hernia

Interventions

DRUG

Ketorolac postoperative

Ketorolac 10mg 1cp x 3/die

DRUG

postoperative Patrol

acetaminophene 325mg+tramadol 37.5mg, 1cp x 3/die

DRUG

intraoperative analgesia

ketorolac 30 mg iv

DRUG

intraoperative analgesia

Tramadol 100 mg if Weight over 50 kg, 50 mg if weight below 50 kg

Sponsors & Collaborators

  • University of Pavia

    collaborator OTHER

  • Fondazione IRCCS Policlinico San Matteo di Pavia

    lead OTHER

Principal Investigators

  • Fabrizio Cavalloro, MD · IRCCS Policlinico San Matteo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2012-05-31
Completion
2012-05-31

Countries

  • Italy

Study Locations

More Related Trials

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 NCT01345162 on ClinicalTrials.gov