Use of Cannabinoids in Patients With Multiple Sclerosis

Multiple Sclerosis Clinical Trial

Official title:

fMRI and Neurophysiological Study Protocol on Cannabinoids in Multiple Sclerosis

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT00202423
• Other study ID #: NEU-CAN-04
• Secondary ID: CRI.FS032
• Status: Recruiting
• Phase: Phase 2
• First received: September 12, 2005
• Last updated: November 28, 2005
• Start date: July 2005

Study information

• Verified date: September 2005
• Source: S. Andrea Hospital
• Contact: Carlo Pozzilli, MD
• Phone: +390649914716
• Email: carlo.pozzilli[@]uniroma1.it
• Is FDA regulated: No
• Health authority: Italy: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

This is a 10-week, randomised, double blind, placebo-controlled, crossover trial to investigate the effect of Cannabis Based Medicine Extract (Sativex) on patterns of brain activation associated with movement in 20 MS patients suffering from lower limb spasticity. Spasticity is a common symptom in Multiple Sclerosis (MS), occurring all over the course of the disease, particularly in the progressive phase.Physiologically, spasticity and hyperreflexia habitually seen in patients with pyramidal syndrome is due to lesions of other descending pathways, such as the cortico reticulospinal pathways, which participate in voluntary movements.It is now known that an endocannabinoid system acts in humans by at least two types of cannabinoids receptors, CB1 and CB2. There is evidence to support the view that the psychoactive ingredient in cannabis, delta 9-tetrahydrocannabinol (delta 9-THC), and cannabinoids in general, can reduce muscle spasticity in people with MS. Aim of the study will be to evaluate the effect of Sativex on: (i) patterns of brain activation associated with movement (fMRI) in MS patients suffering from spasticity; (ii) changes in level of spasticity (H-reflex); (iii) changes in intracortical excitability and on synaptic intracortical network of the motor areas (double shock TMS).

Description:

Baseline assessment will be followed by randomisation and dose introduction. Patients will be randomly assigned to two counterbalanced groups starting either with Sativex or with placebo as the first drug. They will be dispensed sufficient study medication for two weeks together with a diary. During the two-week treatment period all the patients will have to be reached the optimal, individualised dosage to subjectively relief spasticity.Patient will return after three weeks and they will undergo the fMRI and neurophysiological evaluations.Then patients will perform a two-week washout period and they will be requested to intake the alternative medicine. After two weeks patients will perform a second fMRI/neurophysiological study. Two weeks later, after a second washout period, a last visit will be performed to conclude the study.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

1. Male or female subjects between 18 and 60 years of age (inclusive)

2. Have definite Multiple Sclerosis as per Poser Criteria

3. Have either relapsing remitting or secondary progressive course

4. Baseline EDSS score from 3.0 to 6.5 (inclusive)

5. Stable disease for at least 30 days prior to study entry

6. Be right-handed with normal right hand function

7. Female patients of child bearing potential and male patients whose partner is of child bearing potential who are willing to ensure that they or their partner use effective contraception during the study and for three months thereafter

8. If female, be neither pregnant nor breast-feeding. Confirmation that the subjects not pregnant must be established by a negative serum hCG pregnancy test at baseline.

9. No cannabinoids use (cannabis, Marinol, Nabilone) for at least three months prior to entry into the study and willing to abstain from any use of cannabis during the study

10. Significant spasticity in at least two muscle groups defined as a score of 2 or more on the Ashworth scale for each muscle group

11. Antispastic/antiepileptic treatments (dosage, frequency and route of administration) stable for at least one month prior the study entry

Exclusion Criteria:

1. Have a primary progressive MS

2. Patients under disease modifying therapies prescribed in the 6 months prior the study entry

3. Patients who have participated in another research study in the past 6 months

4. Changes in antispastic/antiepileptic treatments (dosage, frequency and route of administration) within one month prior the study entry

5. Have a psychiatric disorders or cognitive impairment that preclude safe participation in the study

6. Known history of alcohol or substance abuse

7. Concurrent clinically important immunologic, pulmonary, renal, liver, active thyroid, and/or other major disease other than MS

8. Severe cardiovascular, disorders, such as ischaemic heart disease, arrhythmias, poorly controlled hypertension or severe heart failure

9. Patients suffering from acute or chronic pain

10. History of epilepsy

11. Female patient who is pregnant, lactating or planning pregnancy during the course of the study

12. Scheduled elective surgery or other procedures requiring general anaesthesia during the study

13. Patient who is terminally ill or is inappropriate for placebo medication

14. Systemic corticosteroid therapy within 4 weeks of randomization or exacerbation of MS within 30 days

15. Regular levodopa therapy within 7 days of the study entry

16. Male patient currently receiving sildenafil (Viagra) and unwilling to stop medication for the duration of the study

17. Patients who are currently taking antiarrhythmic medications

18. Known or suspected adverse reaction to cannabinoids

19. Travel outside the Italy planned during the study

20. Donation of blood during the study

21. Contraindications to MRI scans -

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Multiple Sclerosis
• Sclerosis

Intervention

Drug:
• Sativex

Locations

Country	Name	City	State
Italy	Department of Neurology- University of Rome la Sapienza	Rome

Sponsors (2)

Lead Sponsor	Collaborator
S. Andrea Hospital	University of Roma La Sapienza

Country where clinical trial is conducted

Italy, 

References & Publications (7)

Baker D, Pryce G, Croxford JL, Brown P, Pertwee RG, Huffman JW, Layward L. Cannabinoids control spasticity and tremor in a multiple sclerosis model. Nature. 2000 Mar 2;404(6773):84-7. — View Citation

Pertwee RG. Cannabinoid receptor ligands: clinical and neuropharmacological considerations, relevant to future drug discovery and development. Expert Opin Investig Drugs. 2000 Jul;9(7):1553-71. Review. — View Citation

Smith PF. Cannabinoids in the treatment of pain and spasticity in multiple sclerosis. Curr Opin Investig Drugs. 2002 Jun;3(6):859-64. Review. — View Citation

Vaney C, Heinzel-Gutenbrunner M, Jobin P, Tschopp F, Gattlen B, Hagen U, Schnelle M, Reif M. Efficacy, safety and tolerability of an orally administered cannabis extract in the treatment of spasticity in patients with multiple sclerosis: a randomized, double-blind, placebo-controlled, crossover study. Mult Scler. 2004 Aug;10(4):417-24. — View Citation

Wade DT, Makela P, Robson P, House H, Bateman C. Do cannabis-based medicinal extracts have general or specific effects on symptoms in multiple sclerosis? A double-blind, randomized, placebo-controlled study on 160 patients. Mult Scler. 2004 Aug;10(4):434-41. — View Citation

Wade DT, Robson P, House H, Makela P, Aram J. A preliminary controlled study to determine whether whole-plant cannabis extracts can improve intractable neurogenic symptoms. Clin Rehabil. 2003 Feb;17(1):21-9. — View Citation

Zajicek J, Fox P, Sanders H, Wright D, Vickery J, Nunn A, Thompson A; UK MS Research Group. Cannabinoids for treatment of spasticity and other symptoms related to multiple sclerosis (CAMS study): multicentre randomised placebo-controlled trial. Lancet. 2003 Nov 8;362(9395):1517-26. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To evaluate the effect of Sativex on: a)patterns of brain activation associated with movement(fMRI); b) changes in level of spasticity (H-reflex); c)changes in intracortical excitability and on synaptic intracortical network of the motor areas(TMS).