Skip to main content
OpenTrials
Completed

NCT Number: NCT04634136

Full-spectrum Medical Cannabis for Treatment of Spasticity in Patients With Severe Forms of Cerebral Palsy

The proposed study is a double-blind, placebo-controlled, cross over study on 60 children aged 5 to 25 years with severe spasticity related to cerebral palsy (CP), level IV and V with full-spectrum medical cannabis product of CBD/THC ratio 10:1.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Children, Adult Brain Damage, Chronic Brain Diseases Cannabis Central Nervous System Diseases Cerebral Palsy Chemically-Induced Disorders Marijuana Abuse Mental Disorders Muscle Hypertonia Muscle Spasticity Muscular Diseases Musculoskeletal Diseases Nervous System Diseases Neurologic Manifestations Neuromuscular Manifestations Pathological Conditions, Signs and Symptoms Physical Disability Quality of Life Signs and Symptoms Spastic Cerebral Palsy Substance-Related Disorders

Age range

5 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

PharmaHemp, Ljubljana, Slovenia

Loading trial locations.

About this study

Test components:

A) Active: Full-spectrum medical cannabis with ratio of CBD:THC 10:1 (HemPhar)

B) Placebo (both of the same producer)

Study Steps

  • Informed consent should be signed by parents/caregivers.
  • Weight of the participant should be determined and an IV line inserted. The following lab tests should be performed: CBC and differential counts, blood electrolytes, magnesium, calcium, phosphorus, urea & creatinine, liver enzymes (AST, ALT, gGT)
  • ECG performed and analyzed
  • A trained physiotherapist will perform the following motor assessments: spasticity level according to modified Ashworth scale (Bohannon), function/activity assessment with the use of Gross Motor Function Measure scale (GMFM-88) and assessment of muscle power with dynamometer.
  • Randomization of patients into one of the two arms of the study
  • Active substance or placebo are introduced thereafter (as an oral oily solution for oral application) in a starting dose of 0.08 mg/kg body weight (BWt)/day divided in 2 doses (the dose is according to the THC content). The dose is gradually increased, every 3 days for 0.08 mg THC/ kg BWt/day, until the maximum dose of 1 mg THC/kg BWt/day is reached, or else until adverse effects are noted. It is expected that the average dose will be 0.33 mg/kg BWt per day.
  • The parents/caregivers are given questionnaires/scales and also given oral instructions on how to fulfil them (Edmonton scale, Borg scale and Global Impression of Change - GIC) and the paper to take down notes on possible side/adverse effects while taking the preparation (either active substance or placebo).
  • After 6 weeks of taking the substance or at the premature end of the study again the lab tests will be performed as well as the motor assessment by the physiotherapist (as above at inclusion).
  • In patients, who have been receiving placebo for the first 6 weeks, the active substance is given for the next 6 weeks, as described above (under 6). The patients who have been receiving the active substance for the first 6 weeks will continue to do so for the next 6 weeks.
  • Additional blood samples are taken at 6 weeks in both groups for analysis of levels of cannabidiol (CBD) as well as delta-9-tetrahydrocannbinol (THC) - around 4 ml of blood for determination of both levels at time(s) after ingestion: 0, 1, 2, 4, 8 and 24 hours.
  • At the end of the study (after 12 weeks) again repeat:
  • CBC and differential counts, blood electrolytes, magnesium, calcium, phosphorus, urea & creatinine, liver enzymes (AST, ALT, gGT)
  • ECG
  • Motor assessments by a physiotherapist (Ashworth/Bohannon, GMFM 88, dynamometer)
  • Pharmacokinetics: 4 ml of blood for determination of phamacokinetics after ingestion of the last dose (as in point 10 above)
  • Evaluation of the questionnaires

NOTE: if severe side/adverse effects are noted, the test compound should be stopped immediately. If mild/moderate side/adverse effects are noted, the test component should be gradually stopped: for 0,08 mg/kg BWt/day, every 3 days.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • With confirmed diagnosis of cerebral palsy (CP) and classified according to the Gross Motor Function Classification System (GMFCS) as level IV or V
  • With spastic unilateral or spastic bilateral type of CP
  • Those children/young adults whose parents/caregivers were informed about the aims of the study and have signed the Informed consent form

Exclusion criteria

  • Other proven diseases/conditions with the prevalence of spastic type of muscle tone (e.g. neurodegenerative, metabolic, etc.), and children with liver disease
  • Other forms of CP (dyskinetic, ataxic)
  • History of psychiatric illness/condition in the family

Treatment and study plan

Lab tests

Diagnostic Test

CBC and differential counts, blood electrolytes, magnesium, calcium, phosphorus, urea & creatinine, liver enzymes (AST, ALT, gGT)

Other names: Basic hematology and biochemistry

ECG

Diagnostic Test

Electrocardiogram

Cannabinoid Levels

Diagnostic Test

Determination of levels of cannabidiol (CBD) and delta-9-tetrahydrocannbinol (THC) for determination of levels at following time(s) after ingestion: 0, 1, 2, 4, 8 and 24 hours.

Other names: Pharmacokinetics of cannabinoids

Full-spectrum Medical Canabis Product (HemPhar)

Drug

Active substance

Other names: Active substance

Placebo

Drug

Placebo

Spasticity level according to modified Ashworth scale (Bohannon)

Diagnostic Test

A trained physiotherapist will assess spasticity level according to modified Ashworth scale (Bohannon), which is 6-level scale for assessment of spasticity.

Modified Ashworth/Bohannon Scoring Scale (Bohannon and Smith, 1987):

0 No increase in muscle tone

  • Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+ Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the range of movement (ROM )
  • More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
  • Considerable increase in muscle tone, passive movement difficult
  • Affected part(s) rigid in flexion or extension

Best score is 0 (no spasticity), worst score is 4 (severe spasticity).

Gross Motor Function Measure

Diagnostic Test

A trained physiotherapist will assess Gross Motor Function Measure (GMFM-88) which is commonly used in the evaluation of gross motor function in children with cerebral palsy

The Gross Motor Function Measure-88 (GMFM-88) is a standardized observational instrument developed to measure change in gross motor function over time. The test consists of 88 items categorized in five dimensions (Dimension A: lying and rolling, Dimension B: sitting, Dimension C: crawling and kneeling, Dimension D: standing and Dimension E: walking, running and jumping). The test was conducted as described in the GMFM-88 manual . A percentage score as compared to maximum is calculated for each dimension and for the total score of the five dimensions.

Reference curves exist for GMFM-88 for each age group.

Floor score is 4 (minimum score / worst), ceiling score (maximum score / best) is 75.

Borg rating of perceived exertion scale

Diagnostic Test

Borg rating of perceived exertion scale

Edmonton symptom assessment system

Diagnostic Test

Edmonton symptom assessment system and general impression scale (1 - very much improved; 7 - very much worse).

Primary outcomes

  1. Effect on spasticity (6w; FSMC vs placebo)

    Time frame: 6 weeks

    A trained physiotherapist will assess spasticity level according to modified Ashworth scale (Bohannon), which is 6-level scale for assessment of spasticity.

    Modified Ashworth/Bohannon Scoring Scale (Bohannon and Smith, 1987):

    0 No increase in muscle tone

    • Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+ Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the range of movement (ROM )
    • More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
    • Considerable increase in muscle tone, passive movement difficult
    • Affected part(s) rigid in flexion or extension

    Best score is 0 (no spasticity), worst score is 4 (severe spasticity).

  2. Effect on Gross Motor Function Measure (6w; FSMC vs placebo)

    Time frame: 6 weeks

    A trained physiotherapist will assess Gross Motor Function Measure (GMFM-88) which is commonly used in the evaluation of gross motor function in children with cerebral palsy

    The Gross Motor Function Measure-88 (GMFM-88) is a standardized observational instrument developed to measure change in gross motor function over time. The test consists of 88 items categorized in five dimensions (Dimension A: lying and rolling, Dimension B: sitting, Dimension C: crawling and kneeling, Dimension D: standing and Dimension E: walking, running and jumping). The test was conducted as described in the GMFM-88 manual . A percentage score as compared to maximum is calculated for each dimension and for the total score of the five dimensions.

    Reference curves exist for GMFM-88 for each age group.

    Floor score is 4 (minimum score / worst), ceiling score (maximum score / best) is 75.

  3. Effect on spasticity (12w; 12w-FSMC vs 6w-FSMC)

    Time frame: 12 weeks

    A trained physiotherapist will assess spasticity level according to modified Ashworth scale (Bohannon), which is 6-level scale for assessment of spasticity

    Modified Ashworth/Bohannon Scoring Scale (Bohannon and Smith, 1987):

    0 No increase in muscle tone

    • Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+ Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the range of movement (ROM )
    • More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved
    • Considerable increase in muscle tone, passive movement difficult
    • Affected part(s) rigid in flexion or extension

    Best score is 0 (no spasticity), worst score is 4 (severe spasticity).

  4. Effect on Gross Motor Function Measure (12w; 12w-FSMC vs 6w-FSMC)

    Time frame: 12 weeks

    A trained physiotherapist will assess Gross Motor Function Measure (GMFM-88) which is commonly used in the evaluation of gross motor function in children with cerebral palsy.

    The Gross Motor Function Measure-88 (GMFM-88) is a standardized observational instrument developed to measure change in gross motor function over time. The test consists of 88 items categorized in five dimensions (Dimension A: lying and rolling, Dimension B: sitting, Dimension C: crawling and kneeling, Dimension D: standing and Dimension E: walking, running and jumping). The test was conducted as described in the GMFM-88 manual . A percentage score as compared to maximum is calculated for each dimension and for the total score of the five dimensions.

    Reference curves exist for GMFM-88 for each age group.

    Floor score is 4 (minimum score / worst), ceiling score (maximum score / best) is 75.

  5. Safety and tolerability of FSMC

    Time frame: 12 weeks

    Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]

Sponsors and collaborators

Lead sponsor

University Medical Centre Ljubljana

Other

Collaborators

  • PharmaHemp
  • University of Ljubljana, Faculty of Medicine

Registry information

Official study title

Full-spectrum Medical Canabis Product (HemPhar) With a CBD:THC Ratio of 10:1 for Treatment of Spasticity in Children and Young Adults With Severe Forms of Cerebral Palsy

Acronym: HemPhar

Important dates

Study start
2020
Primary completion
2023
Study completion
2024
First posted
Nov 18, 2020
Registry last updated
May 22, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.