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OpenTrials
Completed

NCT Number: NCT00925847

Effect of Lithium Carbonate in Patients With Amyotrophic Lateral Sclerosis

The purpose of the study is to determine whether lithium is safe and effective in the treatment of ALS

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Pitié-Salpêtrière Hospital

Paris, 75013, France

About this study

Daily doses of lithium, have been found to delay progression of amyotrophic lateral sclerosis (ALS) in a 15-month study of 44 patients with ALS. At the end of the trial, about 30 percent of the patients that took riluzole had died, while all those receiving riluzole plus lithium had survived. the lithium group had slower progression as measure by a test of breathing (FVC) and strength.

This study will determine whether lithium in combination with riluzole delay progression of patients with amyotrophic lateral sclerosis disease in comparison of an historical cohort of ALS patients treated with riluzole alone.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis of clinically possible, clinically probable laboratory-supported, clinically probable or clinically definite ALS (according to WNF EL Escorial diagnostic criteria, revised according to the AIRLIE House Conference 1998)
  • Concomitant standard Riluzole therapy (50mg twice daily)
  • patients included in ALS reference center
  • women of childbearing age be non-lactating and surgically sterile or using a highly effective method of birth control and have a negative pregnancy test
  • capable of thoroughly understanding all information given and giving full informed consent according to GCP
  • Patients with gastrostomy

Exclusion criteria

  • evidence of major psychiatric disorder or clinically evident dementia precluding evaluation of symptoms
  • any medical condition known to contre-indicate lithium treatment (dysthyroid, cardiopathy, renal insufficiency)
  • presence of any concomitant life-threatening disease or impairment likely to interfere with functional assessment
  • known hypersensitivity to any component of the study drugs

Treatment and study plan

Lithium

Drug

lithium LP 400mg daily po (doses were adjusted during the study to maintain targeted blood levels.)

Primary outcomes

  1. Survival in patients with ALS treated with lithium and riluzole compared to historical cohort (patients treated with riluzole alone )

    Time frame: 15 months

Secondary outcomes

  1. Functional Assessment Change in ALS Functional Rating Score (ALSFRS-R slope)

    Time frame: 15 months

  2. Muscle Strength Change in MMT score (MMT slope)

    Time frame: 15 months

  3. Rate of decline of respiratory function determined as SVC over the 15 month treatment period

    Time frame: 15 months

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Open Multicenter Study of Lithium in Patients With Amyotrophic Lateral Sclerosis LISLA

Acronym: LISLA

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Jun 22, 2009
Registry last updated
Oct 31, 2012

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.

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