Administration of magnesiumsulphate has the potential to elicit muscle relaxation. We hypothesize administration of intramuscular magnesiumsulphate can reduce CRPS-related dystonia.
ID
Bron
Verkorte titel
Aandoening
Dystonia in complex regional pain syndrome type 1.
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Primary outcome is severity of dystonia using the Burke-Fahn-Marsden scale.
Achtergrond van het onderzoek
A large proportion of chronic patients with complex regional pain syndrome type 1 (CRPS I) suffer from both neuropathic pain and dystonia. Findings from neurophysiological and intrathecal baclofen (ITB) studies highlight an impaired inhibitory neurotransmission. Since magnesium plays an important inhibitory role in motor regulation, magnesium administration may offer new options for the treatment of movement disorders in patients with CRPS I. Primary aim of the study is to evaluate the efficacy and safety of intramuscular magnesium (IMMG) in CRPS I in a double-blind randomised placebo-controlled cross-over manner.
Doel van het onderzoek
Administration of magnesiumsulphate has the potential to elicit muscle relaxation. We hypothesize administration of intramuscular magnesiumsulphate can reduce CRPS-related dystonia.
Onderzoeksopzet
One week before first injection until 7 weeks after first injection:
1. Self-assessment every day;
2. Other assessments once every week.
Onderzoeksproduct en/of interventie
Intramuscular magnesiumsulphate:
1. Week 1: 500 mg twice a day;
2. Week 2: 750 mg twice a day;
3. Week 3: 1000 mg twice a day.
Publiek
A.A. Plas, v.d
Leiden University Medical Center, Department of Neurology, K5Q,
P.O.Box 9600
Leiden 2300 RC
The Netherlands
+31 (0)71 526 6065
A.A.van_der_Plas@lumc.nl
Wetenschappelijk
A.A. Plas, v.d
Leiden University Medical Center, Department of Neurology, K5Q,
P.O.Box 9600
Leiden 2300 RC
The Netherlands
+31 (0)71 526 6065
A.A.van_der_Plas@lumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Patients must fulfill the diagnostic criteria of the consensus report of CRPS I:
A. Continuing pain, allodynia or hyperalgesia, in which the pain is disproportionate to any inciting event, and;
B. Evidence at some time of edema, changes in skin blood flow or abnormal sudomotor activity in the region of the pain, and;
C. No condition that would otherwise account for the degree of pain and dysfunction.
2. Patients must suffer from clinically significant tonic or intermittent dystonia in one or more extremities;
3. Patients must have symptoms for at least 1 year.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Patients are excluded if they can obtain satisfactory relief of symptoms with conventional treatments;
2. Patients with a history of alcohol or drugs abuse within the past year;
3. Patients with clinically significant psychiatric illness;
4. Pregnant, nursing women and females of childbearing potential not using effective contraception;
5. Patients who are unlikely to comply with study requirements or have a history of poor compliance to medical regimens or study requirements;
6. Patients with an insufficient command and understanding of the Dutch language;
7. Patients involved in legal proceedings (claiming compensation for their CRPS I);
8. Patients with impaired coagulation;
9. Patients with impaired renal function (i.e. serum creatinine below 10 or exceeding 80 µmol/l);
10. Patients with hypermagnesaemia (i.e. total serum Mg exceeding 1.10 mmol/l);
11. Patients requiring the use of diuretics.
Opzet
Deelname
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL1763 |
| NTR-old | NTR1873 |
| Ander register | NL26827.058.09 ( Centrale Commissie Mensgebonden Onderzoek) : P09.021 (METC AMC) |
| ISRCTN | ISRCTN wordt niet meer aangevraagd. |