Oral Prednisone Taper Versus Placebo for the Treatment of Acute Relapses in Multiple Sclerosis

Phase 4

Terminated

• Conditions: Multiple Sclerosis
• Interventions: Drug: Placebo; Drug: Prednisone

• Registration Number: NCT01411514
• Lead Sponsor: Claudio Gobbi

Brief Summary

The management of MS-patients requires treatment with immune-modifying or immune-suppressive agents to prevent new relapses and progression of disability. Several studies have evaluated the effect of steroid treatment on clinical recovery after an acute relapse. An important unanswered clinical question is, whether or not an oral tapering dose of corticosteroids offers any additional advantage over intravenous methylprednisolone alone in improving neurologic recovery as well as safety and tolerability after a relapse.

This study aims to compare the efficacy, tolerability and safety of tapering doses of oral prednisone and placebo after short-term high-dose i.v. methylprednisolone on the recovery from an acute relapse in patients with clinically isolated syndrome (CIS), relapsing-remitting multiple sclerosis (RR-MS) and primary (PP-MS) or secondary progressive multiple sclerosis (SP-MS) with superimposed relapses.

Patients will be treated during 25 days with de-escaling doses of prednisone or placebo.

The primary analysis will test whether placebo is equivalent to oral prednisone taper on the recovery status as measured by EDSS change from baseline to 3 months after baseline.

Detailed Description

The purpose of this double-blind, randomised, placebo-controlled, prospective, parallel group, single centre study is to evaluate the effect of tapering oral doses of prednisone or placebo taken during 25 days following short-term high-dose i.v. methylprednisolone on the outcome of a relapse in patients with CIS; RR-MS, PP-MS or SP-MS with superimposed relapses. The primary objective is to assess and compare the recovery status in both patient groups 3 months after baseline by means of Expanded Disability Status Scale (EDSS). Secondary objectives are the assessments of clinical parameters at the end of oral treatment, 6, 9 months after baseline, of MRI markers, of mental and cognitive status, quality of life and fatigue at the end of oral treatment, 3 and 6 months after baseline in both patient groups.

After standard treatment of an acute clinical relapse with high dose, short term i.v. methyprednisolone patients will be randomised to one of the two treatment arms. Patients allocated to prednisone will be treated with tapering oral doses during 25 days. The initial dose of 60 mg will be reduced twice by 20 mg, than by 10 and 5 mg. Each dose regimen will be taken during 5±2 days. Patients randomised to placebo will receive placebo treatment during 25 days.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2011-05-26
• Study Start: 2011-08
• Study First Submitted QC: 2011-08-05
• Study First Posted: 2011-08-08
• Primary Completion: 2015-01
• Study Completion: 2015-01
• Status Verified: 2015-12
• Last Update Submitted: 2015-12-17
• Last Update Posted: 2015-12-18

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 27

Inclusion Criteria

• female or male
• aged between 18 and 80 years;
• with relapsing forms of multiple sclerosis diagnosed according to McDonald's criteria, including RR-MS and relapsing SP-MS, CIS, PP;
• with EDSS score between 0 and 8;
• experiencing an acute relapse with a documented clinical worsening of at least one point of the EDSS scale or a worsening of at least 2 points in one of the EDSS functional systems;
• having agreed to have MRI and having already received at least one enhanced MRI before study procedures without major side effects;
• having agreed to adhere to the study procedures;
• having signed the written informed consent form.

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Exclusion Criteria

• secondary progressive MS without superimposing relapses;

• primary progressive MS without superimposed relapses;

• patients suffering from any clinical condition contraindicated for steroid, in particular

  • Systemic fungal infection
  • Severe osteoporosis
  • Uncontrolled hypertension or congestive heart failure.
  • Existing or previous history of severe affective disorders (especially previous steroid psychosis).
  • Diabetes mellitus
  • History of tuberculosis
  • Glaucoma
  • Previous corticosteroid-induced myopathy
  • Liver failure or cirrhosis
  • Renal insufficiency
  • Active epilepsy
  • Peptic ulceration
  • Fresh intestinal anastomoses
  • Predisposition to thrombophlebitis
  • Abscess or other pyogenic infections
  • Diverticulitis
  • Myasthenia gravis
  • Ocular herpes simplex
  • Hypothyroidism
  • Recent myocardial infarction
  • Kaposi's sarcoma;

• any disease other than multiple sclerosis that would better explain the patient's signs and symptoms;

• women of potential childbearing without active contraceptive methods;

• pregnancy (urine pregnancy test at baseline visit) or breast feeding;

• history of affective disorders;

• history of attempted suicide or current suicidal ideas;

• medical or psychiatric conditions that compromise the ability to give informed consent, to comply with the protocol, or to complete the study;

• inability, in the opinion of the principal investigator or staff, to comply with protocol requirements for the duration of the study;

• known hypersensitivity to prednisone or excipients of the study medications;

• any contraindication for concomitant medications;

• any contraindication for MRI or contrast administration;

• a history of drug abuse in the 6 months prior to screening;

• use of steroids during the previous 30 days (disease-modifying therapies for the treatment of MS are allowed);

• treatment with drugs that might interfere with the evaluation of study drugs during the study protocol (see Section 4.2.2);

• likelihood of requiring treatment during the study period with drugs not permitted by the study protocol;

• participation in an other clinical trial within 30 days prior to entry in this study or current participation in another trial.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo	Placebo	-
Prednisone	Prednisone	-

Primary Outcome Measures

Name	Time	Method
Expanded Disability Status Scale (EDSS)	baseline, 3 months	The scores of the Expanded Disability Status Scale (EDSS) will be assessed at baseline, defined as start of oral treatment with prednisone or placebo (Day 1), and 3 months after baseline.

Secondary Outcome Measures

Name	Time	Method
Euroqol-5D (EQ-5D	baseline, 6 months	patient reported quality of life
Expanded Disability Status Scale (EDSS)	baseline, 9 months	The scores of the Expanded Disability Status Scale (EDSS) will be assessed at baseline, defined as start of oral treatment with prednisone or placebo (Day 1), and 9 months after baseline.
Multiple Sclerosis Functional Composite Score (MSFC)	baseline, 9 months	the Multiple Sclerosis Functional Composite Score (MSFC) includes the Timed 25 foot-walk-test, the 9 Hole Peg test and Paced Auditorial Addition Test (PASAT)
mental status (MUSIC)	baseline, 6 months	investigator administered questionnaire
Gd-enhancing lesions on T1-weighted images	baseline, 6 months	the evolution of the number of Gd-enhancing lesions on T1-weighted images will be assessed
number of new T2-hyperintense lesions	baseline, 6 months	the evolution of the number of new T2-hyperintense lesions will be assessed
Functional Assessment Multiple Sclerosis (FAMS)	at baseline, 6 months	Patient reported outcome
Fatigue Scale for Motor and Cognitive functions (FSMC)	baseline, 6 months	Investigator administered questionnaire
Beck Depression Inventory Second edition (BDI-II)	baseline, 6 months	Investigator administered questionnaire

Trial Locations

Locations (1)

Osepdale Civico; 🇨🇭 Lugano, Ticino, Switzerland