Postoperative Relapses in MS Patients

January 19, 2020 updated by: Staikou Chryssoula, University of Athens

Assessment of Risk of Postoperative Relapses in Patients With Multiple Sclerosis; an Observational Study

The aim of the study is to record any relapses during one year postoperatively in patients and parturients diagnosed with MS who received general or regional anesthesia

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Anticipated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Chryssoula V Staikou, Assoc Prof
  • Phone Number: 00302107780172
  • Email: c_staikou@yahoo.gr

Study Locations

  • Greece
      • Athens, Greece
        • Recruiting
        • Aretaieio Hospital
        • Contact:
          • Chryssoula V Staikou, Assoc Prof
    • Attiki
      • Athens, Attiki, Greece, 11528
        • Recruiting
        • Aretaieio Hospital, University of Athens

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 70 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

patients or parturients with MS who received general or regional anesthesia for surgery or labor analgesia

Description

Inclusion Criteria: diagnosed MS -

Exclusion Criteria: refuse to participate

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
general anesthesia
Procedure: surgery and anesthesia
patients with MS who received general or regional anesthesia for a surgery or labor
regional anesthesia
Procedure: surgery and anesthesia
patients with MS who received general or regional anesthesia for a surgery or labor

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
MS relapses
Time Frame: one year postoperatively
number of relapses
one year postoperatively

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Athens

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

December 20, 2019

Primary Completion (ANTICIPATED)

December 1, 2027

Study Completion (ANTICIPATED)

December 1, 2027

Study Registration Dates

First Submitted

January 19, 2020

First Submitted That Met QC Criteria

January 19, 2020

First Posted (ACTUAL)

January 23, 2020

Study Record Updates

Last Update Posted (ACTUAL)

January 23, 2020

Last Update Submitted That Met QC Criteria

January 19, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 157/19-12-19

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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