Skip to main content
OpenTrials
Completed

NCT Number: NCT02381444

Health Related Quality of Life in LCIG Patients and LCIG Eligible Patients Continuing Oral Therapy

The aim of this study is to assess the effect of LCIG (levodopa-carbidopa intestinal gel) on HRQL (Health-Related Quality of Life) of participants and compare the Health-Related Quality of Life between participants continuing to levodopa-carbidopa intestinal gel treatments versus participants continuing on oral therapy for Parkinson's Disease.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Universitaetsklinikum Aachen /ID# 204355, Aachen, North Rhine-Westphalia, Germany

Loading trial locations.

About this study

Parkinson's disease (PD) is the second most common neurodegenerative disorder in the world. It can be treated sufficiently until motor complications with fluctuations of mobility and dyskinesia develop. The quality of life is relentlessly deteriorating with longer disease duration once the complications of conservative oral therapy develop. Continuous dopaminergic stimulation using Levodopa/Carbidopa Intestinal Gel (LCIG) improves the motor complications of Parkinson's disease and preliminary data suggest that also the quality of life is improved. Primary Objective is to assess the effect of LCIG on Health Related Quality of Life (HRQL) of patients according to selection criteria from German guidelines and compare improvement in HRQL between patients continuing to LCIG treatment and patients staying on oral treatment, despite being eligible according to these guidelines. In addition, current selection criteria recommended by the national guideline will be documented at baseline.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Eligibility for LCIG according to current version of the Summary of Product Characteristics of LCIG of the respective country (Germany, Switzerland).
  • Decision to treat with LCIG or other medication made by the study physician prior to any decision to approach the patient to participate in this study.
  • Unchanged available combinations of PD medicinal treatment for at least one week prior to study inclusion.
  • Patient has given written informed consent.

Exclusion criteria

  • Contraindication to LCIG according to current version of the German SmPC or Swiss SmPC.
  • Contraindication to placement of intrajejunal PEG-J tube.
  • Current treatment with Deep Brain Stimulation (DBS), Apomorphine pump or LCIG
  • Severe dementia based on a Mini-Mental State Examination (MMSE) of < 10
  • Acute psychotic disorder (benign hallucinations or earlier psychotic episodes are not an exclusion criterion)
  • Depression with suicidal thoughts (earlier episodes of major depression are not an exclusion criterion)
  • History or presence of any condition that might interfere with absorption, distribution, metabolism, or excretion of LCIG
  • Drug or alcohol addiction (drug addiction: continuous or sporadic use of drugs without medical indication or with paradoxical medical indication or in inappropriate amounts. Addictive consumption of e.g. alcohol, cannabis, amphetamine, sniffing agents, cocaine, heroin, crack). Alcohol addiction male: > 40 g/day; female: > 30 g/day)
  • Illiteracy or insufficient language skills to complete the questionnaires

Treatment and study plan

Primary outcomes

  1. Change in the Parkinson's Disease Questionnaire (PDQ-39) summary index

    Time frame: From baseline to 12 months

    The primary endpoint is the change in the Parkinson's Disease Questionnaire (PDQ-39) summary index from 12 months to the baseline assessment. The two treatment groups levodopa-carbidopa intestinal gel vs. Standard of Care will be compared.

Secondary outcomes

  1. Change in Health Related Quality of Life (HRQL)

    Time frame: At Baseline, 6, and 12 months of treatment

    Unified Parkinson's disease Rating Scale (UPDRS) part III in the medication "on" state

  2. Change in participant's motor symptoms

    Time frame: From Baseline to 6 and 12 months of treatment.

    Activities of daily living "on" and "off" medication - Unified Parkinson's disease Rating Scale (UPDRS) part II

  3. Change in participant's Healthcare Resource Utilization

    Time frame: From Baseline to 6 and 12 months of treatment

    Frequency and severity of ON-dyskinesia (Unified Parkinson's Disease Rating Scale part IV, Complications of Therapy: Items 32, 33, 34 and 39)

  4. Change in participant's non-motor symptoms

    Time frame: From baseline to 6 and 12 months of treatment

    Non Motor Symptoms Scale (NMSS) Total score and subdomains Cardiovascular, Sleep/Fatigue, Gastrointestinal, Urinary, Sexual functioning

  5. Reason for transition to LCIG (or continuing oral therapy)

    Time frame: At Baseline, 6 and 12 month

    There are no data comparing long-term HRQL of LCIG versus peroral therapy

  6. Change in participant's caregiver burden

    Time frame: From Baseline to 6 and 12 months of treatment

    Non Motor Symptoms Scale (NMSS) Total score and subdomains Cardiovascular, Sleep/Fatigue, Gastrointestinal, Urinary, Sexual functioning

Sponsors and collaborators

Lead sponsor

AbbVie

Industry

Registry information

Official study title

Health Related Quality of Life in LCIG Patients and LCIG Patients and LCIG Eligible Patients Continuing Oral Therapy. A Multicenter Post Marketing Observational Study for LCIG in Germany and Switzerland - BALANCE

Acronym: BALANCE

Important dates

Study start
2015
Primary completion
2020
Study completion
2020
First posted
Mar 6, 2015
Registry last updated
Dec 9, 2020

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.

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