Postoperative Relapses in MS Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorUniversity of Athens

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

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

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • surgery and anesthesia

    Procedure/Surgery

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

Treatment groups

300 Participants
are divided into 2 treatment groups
Group A: regional anesthesia1 intervention
Group B: general anesthesia1 intervention

Trial outcomes

Primary outcomes

1

MS relapses

number of relapses

Time frame
one year postoperatively

Secondary outcomes

Other outcomes

Sponsors and contacts

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