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Completed

NCT Number: NCT02940912

Effect of Continuous Apomorphine During the Night on Sleep Disorders in Insomniac Patients With Parkinson's Disease

The purpose of the study is to demonstrate that continuous apomorphine treatment during the night compared with placebo improves sleep quality in insomniac patient with Parkinson's disease.

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Key information

About this study

Sleep disorders are very common in Parkinson's disease (PD). They are present in almost all patients. They have an important impact on quality of life. To improve the comfort of patients, neurologists typically offer either dispersible form of levodopa, prolonged release dopaminergic agonists treatments or deep brain stimulation surgery. Unfortunately these treatments are too short-acting for the dispersible form of levodopa or not always sufficient for the oral or transdermal dopamine agonist or are very heavy to implement as surgery.

Some sleep disorders such as restless legs syndrome and periodic leg movements, and obstructive sleep apnoea syndrome, seem to be more frequent in PD patients than in general population and could be improved by a continuous dopaminergic treatment the night.

Finally, daytime sleepiness is a major problem in PD patients. Although it seems most often linked to dopaminergic treatments given during the day, it could also be, in some patients the result of a very bad night's sleep, leading to a rebound of sleep during the day.

The main objective is to demonstrate that compared with placebo, nocturnal continuous apomorphine treatment improves sleep quality assessed by the patient on the PDSS-2 scale in fluctuating parkinsonian patients with complaints of insomnia.

The secondary objectives are to measure the effectiveness of nocturnal continuous apomorphine on sleep quality : total sleep time, sleep efficiency, arousal index, ventilatory events and legs movements indexes, to measure the relative proportion of sleep stages (N1, N2, N3, Rapid Eye Movement ou REM sleep), position changes during sleep index and the percentage of time spent in the supine position, percentage of time with SpO2 <90%), sleepiness (Epworth and Multiple Sleep Latency Test) and their consequences on quality of life (EuroQol 5), depressive symptoms (Beck II), anxiety (STAI), overall cognition (MOCA), pain and engine condition after waking up.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Idiopathic Parkinson's disease ( Hughes AJ et al. 2001)
  • Patients with motor fluctuations
  • Chronic Insomnia disorder criteria according to the criteria of DMS- V ( American Psychiatric Association, 2013) and insomnia severity index > 15
  • Able to use independently the device required for treatment by apomorphine
  • Collection of written informed consent (legal obligation for any project under the public health law , bioethics laws and / or CNIL) .
  • Affiliate to social security or beneficiary of such a regime

Exclusion criteria

  • Atypical Parkinsonian Syndromes
  • Parkinson's disease with dementia (Montreal Cognitive Assessment (MoCA) <25/30 (NASREDDINE and al., 2012))
  • Parkinson's disease with hallucinations
  • Parkinson's disease with impulse Control disorder (ICD)
  • Parkinson's disease already treated with APOMORPHINE pump or justifying the use of the pump continuously day and night
  • Another obvious severe disease explaining insomnia
  • Exclusion for monitoring difficulties (mutation, insufficient motivation, priority associated pathology in care)
  • Patient unwilling to accept a pump
  • Patient not accepting polysomnography and multiple sleep latency test
  • Patient with health problems or a skin disease precluding continuous subcutaneous infusion
  • Female parturient or nursing
  • Cardiac dysrhythmia precluding treatment with domperidone or apomorphine (increased QTc ≥ 440 ms in men, QTc ≥ 450 ms in women)
  • Treatments forbidden in association with apomorphine such as:
  • antiemetic neuroleptics
  • Tetrabenazine
  • Excessive alcohol consumption
  • Contraindications for apomorphine:
  • Hypersensitivity to apomorphine or one of the excipients
  • Respiratory Depression
  • Hepatic impairment
  • Intellectual Disability
  • Dementia

Treatment and study plan

Apomorphine

Drug

cross-over with start with Apokinon in the 1st phase- in the 2nd phase of continuous treatment with Physiologic Serum.

Other names: Apokinon

Placebo

Drug

cross-over with start with.Physiologic Serum in the 1st phase- in the 2nd phase of continuous treatment with Apokinon.

Other names: Physiologic Serum

Primary outcomes

  1. Change from baseline PDSS2 score (Parkinson's Disease Sleep Scale) at the end of the sequence

    Time frame: 53 days

    This score is a score range, it's the difference between PDSS2 score at day18 and day 1 (for the first sequence) and difference between day 53 and day 36 (for the second sequence).

Secondary outcomes

  1. Total sleep time period

    Time frame: 53 days

    Variable will be measured from the polysomnography recordings

  2. Total sleep time (non-Rapid Eye Movements (REM) stages 1,2,3 plus REM sleep)

    Time frame: 53 days

    Variables will be measured from the polysomnography recordings

  3. Length of the intra-sleep wakefulness

    Time frame: 53 days

  4. Sleep efficiency (total sleep time based on the total sleep period)

    Time frame: 53 days

  5. Duration of each sleep stage of the total sleep time

    Time frame: 53 days

  6. Subjective sleepiness on the Epworth Sleepiness Scale

    Time frame: 53 days

  7. Sleep latency (between light extinction and the first period of sleep)

    Time frame: 53 days

  8. Arousal index

    Time frame: 53 days

  9. Apnea / hypopnea Index

    Time frame: 53 days

  10. Percentage of time spent with a saturation below 90%

    Time frame: 53 days

  11. Periodic leg movement index

    Time frame: 53 days

  12. Percentage of REM sleep time with tonic and phasic activity

    Time frame: 53 days

  13. Objective sleepiness on Multiple Sleep Latency Test

    Time frame: 53 days

Sponsors and collaborators

Lead sponsor

Clinique Beau Soleil

Other

Registry information

Official study title

Double Bind Randomized Placebo-controlled Cross-over Study to Evaluate Effect of Continuous Apomorphine During the Night on Sleep Disorders in Insomniac Patients With Parkinson's Disease

Acronym: APOMORPHEE

Important dates

Study start
2017
Primary completion
2021
Study completion
2021
First posted
Oct 21, 2016
Registry last updated
Apr 25, 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.

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