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NCT02864004CompletedPhase 3

Apomorphine Pump in Early Stage of Parkinson's Disease (EARLY-PUMP)

Apomorphine Pump in Early Stage of Parkinson's Disease

Source: ClinicalTrials.gov · Last updated 16 Jun 2026

Brief summary (registry, in English)

The aim of the study is to assess the use of the apomorphine pump in earlier stages of Parkinson' Disease (PD), when motor complications have just developed and before patients are significantly affected in their social and occupational functioning. The investigators hypothesize that apomorphine pump is superior in terms of positive impact on quality of life (QoL) to oral medical therapy alone at a relatively early stage of PD, before the appearance of severe disabling motor complications thus favoring the maintain of patients' social and occupational status with a significant positive economic impact of the health system.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
134 (actual)
First submitted
15 Jul 2016
Start date
3 Mar 2017
Primary completion date
12 Jan 2024
Lead sponsor
Rennes University Hospital
NCT number
NCT02864004

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 134
  • From 3 Mar 2017 to the primary completion date, 12 Jan 2024
  • 20 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous use of apomorphine pump treatment,
  • Concomitant therapy or within 28 days prior to baseline with : alpha-methyl dopa, metoclopramide, reserpine, neuroleptics (except Clozapine), methylphenidate, or amphetamine, intrajejunal Ldopa,
  • History or current drug or alcohol abuse or dependencies,

Other illness

  • Dementia (MoCA \< 22),
  • Major uncontrolled depression at the time of assessment (BDI \> 25) or Bipolar disease,
  • Active hallucinations or history of hallucinations in the past year,
  • History of respiratory depression,
  • History of deep brain stimulation or lesional surgery for PD or intrajejunal L-Dopa,
  • Hypersensitivity to apomorphine or any excipients of the medicinal product,

Lab values

  • Clinically relevant hepatic dysfunction (total bilirubin \>2.0 mg/dL, Alanine Amino Transferase (ALT) and Aspartate Amino Transferase (AST) \>2 times the upper limit of normal),
  • Clinically relevant renal dysfunction (serum creatinine \>2.0 mg/dL),
  • Patients with a borderline QT interval corrected for heart rate according to Bazett's formula (QTc) of \>470 ms for male and \>480 ms for female at screening or history of long QT syndrome;

Other

  • Need for nursing care,
  • Presence of severe freezing or clinically relevant postural instability leading to falls during the ON state,
  • Symptomatic clinically relevant and medically uncontrolled orthostatic hypotension,
  • Pregnant and breastfeeding women,
  • Adults legally protected (under judicial protection, guardianship or supervision), persons deprived of their liberty.

Who the study is looking for

  • Adults aged ≤ 65 years,
  • Idiopathic PD (According to British Brain Bank Criteria) without any other known or suspected cause of Parkinsonism,
  • Hoehn and Yahr stage ≤ 2.5 in the best ON,
  • Disease duration ≥ 4 years,
  • Presence of fluctuations and/or dyskinesias for no more than 3 years,
  • One of the two following forms of impairment :
    • Impairment in activities of daily living (MDS-UPDRS II\>6) due to PD-symptoms despite medical treatment in the worst condition or,
    • Impairment of social and occupational functioning (measured with SOFAS) due to PD-symptoms despite medical treatment (51-80%),
  • PDQ39 completed,
  • Able to understand and remember the component of the study,
  • Written informed consent,
  • Patients covered with social insurance.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (20)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Amiens University Hospital
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AmiensFranceUnknown status
Bayonne Côte Basque Hospital
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BayonneFranceUnknown status
Pellegrin University Hospital
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BordeauxFranceUnknown status
Pierre Wertheimer Hospital
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BronFranceUnknown status
Caen University Hospital
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CaenFranceUnknown status
Clermont-Ferrand University Hospital
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Clermont-FerrandFranceUnknown status
Lille University Hospital
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LilleFranceUnknown status
APHM, hospital of Timone
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MarseilleFranceUnknown status
Montpellier University Hospital
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MontpellierFranceUnknown status
Clinique Beau Soleil
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MontpellierFranceUnknown status
Nancy University Hospital
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NancyFranceUnknown status
Laennec Hospital
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NantesFranceUnknown status
Pasteur 2 University Hospital
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NiceFranceUnknown status
Caremeau University Hospital
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NîmesFranceUnknown status
Pitié Salpêtrière Hospital
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ParisFranceUnknown status
Poitiers University Hospital
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PoitiersFranceUnknown status
Rennes University Hospital
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RennesFranceUnknown status
Saint-Etienne University Hospital
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Saint-EtienneFranceUnknown status
Hautepierre University Hospital
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StrasbourgFranceUnknown status
Purpan University Hospital
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ToulouseFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.