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Paraspinous Anesthetic Block for Non-Responsive Pelvic Pain

NCT01635205 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2014-04-24

No results posted yet for this study

Summary

This study examines randomized triple-blind clinical trial and the efficacy of paraspinous anesthetic block on the treatment of chronic pelvic pain in patients non-responsive to pharmacological management. Sixty patients will be randomly divided and allocated into group intervention (paraspinous anesthetic block) and control (placebo procedure in subcutaneous tissue).

Conditions

  • Paraspinous Block
  • Pelvis Pain Chronic

Interventions

PROCEDURE

paraspinous anesthetic block

Paraspinous anesthetic block with lidocaine 1% in sensitized segments of the thoracolumbar region

PROCEDURE

subcutaneous puncture with no anesthetic effect

Subcutaneous puncture with injection needle (no substance will be injected)

Sponsors & Collaborators

  • Hospital de Clinicas de Porto Alegre

    lead OTHER

Principal Investigators

  • Karen F Rosa, MD · Hospital de Clínicas de Porto Alegre

  • Antonio C Santos, doctor · Hospital de Clínicas de Porto Alegre

  • Ricardo F Savaris, doctor · Hospital de Clínicas de Porto Alegre

  • Vinícius A Amantéa, MD · Hospital de Clínicas de Porto Alegre

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2013-05-31
Completion
2013-05-31

Countries

  • Brazil

Study Locations

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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 NCT01635205 on ClinicalTrials.gov