Parkinson´s DiseaseNCT01003535
Quantification of Cerebral Cholinergic Function in Parkinson´s Disease by Means of Nuclear Medicine Methods
An observational study of Parkinson´s Disease and Acetylcholine, run by Universität des Saarlandes at 1 site in Germany.
Trial summary
Parkinson´s disease is based on a Lewy body degeneration of cerebral and extracerebral neurons. This Lewy body degeneration includes cerebral cholinergic neurons besides dopaminergic neurons. Read more about this study
- Who is it for?
- Ages 50 to 75 years
- Conditions the study is for
- Parkinson´s Disease, Acetylcholine, SPECT
- How many people
- 25 participants
- Where
- 1 siteGermany
- Study dates
- Jan 2010to Apr 2012
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 50 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients with Parkinson´s disease
Who may be able to join
- patients with Parkinson´s disease (after the UK Brain Bank criteria)
- Hoehn and Yahr stage 1
- age 50 - 75 years
- non-smokers
- informed consent to participate in the study
Who cannot join
- pregnant or nursing women
- no adequate contraception in women who are capable of childbearing
- male patients living with fertile women without adequate contraception
- smokers
- actual or past drug or alcohol abuse
- dementia (minimental state test < 25 points)
Show all 9Show fewer
- psychosis or antipsychotic medication in the last 12 months
- cholinergic or anticholinergic medication
- unstable or severe internal diseases
Trial locations and contacts
1 site in 1 country.
Germany1 site
Department of Neurology, Saarland University
Homburg/Saar, Saarland, D-66421
About this study
Official title: Quantification of Cerebral Cholinergic Function in Patients With Parkinson´s Disease by Means of Nuclear Medicine Methods
Parkinson´s disease is based on a Lewy body degeneration of cerebral and extracerebral neurons. This Lewy body degeneration includes cerebral cholinergic neurons besides dopaminergic neurons.
In previous studies the investigators found that some clinical parkinsonian symptoms - primarily hypokinesia and rigidity - significantly correlate with the dopaminergic nigrostriatal degeneration which was quantified by dopamine transporter imaging. In contrast to that, resting or postural parkinsonian tremor does not correlate with the dopaminergic nigrostriatal degeneration. Obviously further cerebral changes - for instance possible changes / degeneration of cerebral cholinergic neurons - contribute to parkinsonian tremor.
In this study the investigators apply cerebral 5-IA-85380-SPECT to quantify the local density of cerebral nicotinergic cholinergic receptors in patients with Parkinson´s disease. The investigators will correlate the results of cerebral 5-IA-85380-SPECT with the clinical parkinsonian main symptoms hypokinesia, rigidity and primarily resting and postural tremor. In particular, it is of interest whether changes of cerebral cholinergic neurons are involved in the generation of parkinsonian tremor.
Read the detailed description
The protocol of our study - as explained in the following - was approved by the Local Ethics committee (Ethics committee of the medical association of the Saarland, D-66111 Saarbrücken, Germany, file number 201/06) and by the German Federal Agency for Radiation Protection (Bundesamt für Strahlenschutz, D-38201 Salzgitter, Germany, file number Z 5 - 22461/2 2008-207).
Aims of this study:
In this study we measure the density and local distribution of cerebral acetylcholine receptors in patients with Parkinson´s disease (PD) by means of [123I]5-IA-85380 SPECT. [123I]5-IA-85380 SPECT was applied in healthy volunteers (Fujita et al. 2002, Fujita et al. 2003, Ding et al. 2004, Mamede et al. 2004, Obrzut et al. 2005) and PD patients (Fukuyama et al. 2004, Bucerius et al. 2006, Fujita et al. 2006). These numerous previous studies proved that [123I]5-IA-85380 SPECT is a safe and effective method to visualize cerebral acetylcholine receptors.
We intend to correlate the density and distribution of cerebral acetylcholine receptors with the clinical parkinsonian cardinal symptoms tremor, hypokinesia and rigidity. The patients are out-patients who are treated by the Department of Neurology, Saarland University, D-66421 Homburg/Saar, Germany. The nuclear medicine measurement [123I]5-IA-85380 SPECT will be performed in the Department of Nuclear medicine of the University of Würzburg, D-97080 Würzburg, Germany.
This study should answer the following questions:
- Does the density of acetylcholine receptors in putamen, caudate nucleus, thalamus and pons correlate with the severity of the clinical symptoms hypokinesia, rigidity, resting tremor, postural tremor?
- Do PD patients with the tremor dominant type, akinetic rigid type and equivalence type differ concerning their accumulation of 5-IA-85380 (=density of acetylcholine receptors) in the putamen, caudate nucleus, thalamus and pons?
Study protocol:
This study will include 25 patients with Parkinson´s disease (PD), Hoehn and Yahr stage 1. 25 patients have to be included ,if a correlation coefficient r = 0.5, an error 1st order = 0.05 and an error 2nd order = 0.20 are assumed. In addition, the number of 25 patients was sufficient in previous studies to obtain significant results. Due to the stochastic risk of radiation-induced long-term side effects (for example neoplasms), which is higher in younger patients, the lower age limit of included patients is determined to 50 years. The upper age limit is 75 years, since vascular cerebral changes increase exponentially in the higher age. The antiparkinsonian medication - except anticholinergic medication - can be continued during the nuclear medicine examination because previous studies excluded any interference between antiparkinsonian medication - except anticholinergic medication - and 5-IA-85380 SPECT.
The severity of the clinical parkinsonian motor symptoms hypokinesia, rigidity, resting tremor and postural tremor are quantified by means of the motor part of the UPDRS (Unified Parkinson´s Disease Rating Scale). The UPDRS is measured in the "Off"-state; "Off"-state means that the medication was interrupted for at least twelve hours. Further the Mini Mental State-Test and DemTect are measured. Healthy controls are not included since there exist norm values in the literature (Fujita et al. 2002, Fujita et al. 2003, Ding et al. 2004, Mamede et al. 2004, Obrzut et al. 2005).
The tracer [123I]5-IA-85380 is produced in the laboratory of radiochemistry and radiopharmacy of the University of Würzburg at the day of examination. This laboratory has the official permission to produce radiotracers. After informed consent by the patient and thyroid gland blocking with perchlorate, the radioactively marked tracer [123I]5-IA-85380 (185 MBq) was given intravenously. Cerebral SPECT imaging was performed 2-3 hours after intravenous injection of the radioactive substance [123I]5-IA-85380. A triple-head gamma camera equipped with low-energy high-resolution collimators was used. Data was acquired in a 128 x 128 matrix covering 120 degrees per camera and head, 50 seconds per view. A total of 120 views was acquired.
Statistical analysis:
The correlation between density of acetylcholine receptors (= uptake of [123I]5-IA-85380) in different brain regions is correlated with the severity of clinical symptoms. The latter was quantified by the items of the UPDRS score.
Correlations were calculated using the Pearson´s correlation coefficient in case of a normally distributed data and Spearman´s correlation coefficient in case of a not normally distributed data.
- Conditions
- Parkinson´s Disease, Acetylcholine, SPECT
- Keywords
- Parkinson´s disease, Acetylcholine receptors
- Medical subject headings
- Parkinson Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| [123I]5-IA-85380 SPECT | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
Correlation of density of acetylcholine receptors in distinct brain areas versus the clinical parameters resting tremor, postural tremor, hypokinesia and rigidity in patients with Parkinson´s disease
Measured: 1 time
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Oct 2009 (estimated)
- Study startJan 2010
- Primary completionApr 2012
- Study completionApr 2012
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (8)Papers the sponsor has linked to this study.
- Other trials for Parkinson´s DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 25 participants (actual)
Sponsor and investigators
- Lead sponsor
- Universität des Saarlandes
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Joerg Spiegel, Universität des Saarlandes
- Investigators
- Joerg Spiegel, M.D., Principal investigator, Department of Neurology, Saarland University, Kirrberger Strasse, D-66421 Homburg/Saar, Germany
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01003535
- Sponsor's protocol ID
- JoergSpiegel1
- Status last verified
- Jul 2012
- First submitted
- 26 Oct 2009
- Last updated
- 4 Jul 2012
- Results posted
- No
- Data monitoring committee
- No
Publications
Bucerius J, Joe AY, Schmaljohann J, Gundisch D, Minnerop M, Biersack HJ, Wullner U, Reinhardt MJ. Feasibility of 2-deoxy-2-[18F]fluoro-D-glucose- A85380-PET for imaging of human cardiac nicotinic acetylcholine receptors in vivo. Clin Res Cardiol. 2006 Feb;95(2):105-9. doi: 10.1007/s00392-006-0342-6. Epub 2006 Jan 19.
PubMed 16598519Ding YS, Fowler JS, Logan J, Wang GJ, Telang F, Garza V, Biegon A, Pareto D, Rooney W, Shea C, Alexoff D, Volkow ND, Vocci F. 6-[18F]Fluoro-A-85380, a new PET tracer for the nicotinic acetylcholine receptor: studies in the human brain and in vivo demonstration of specific binding in white matter. Synapse. 2004 Sep 1;53(3):184-9. doi: 10.1002/syn.20051. No abstract available.
PubMed 15236351Fujita M, Seibyl JP, Vaupel DB, Tamagnan G, Early M, Zoghbi SS, Baldwin RM, Horti AG, KoreN AO, Mukhin AG, Khan S, Bozkurt A, Kimes AS, London ED, Innis RB. Whole-body biodistribution, radiation absorbed dose, and brain SPET imaging with [123i]5-i-A-85380 in healthy human subjects. Eur J Nucl Med Mol Imaging. 2002 Feb;29(2):183-90. doi: 10.1007/s00259-001-0695-z.
PubMed 11926380Fujita M, Ichise M, van Dyck CH, Zoghbi SS, Tamagnan G, Mukhin AG, Bozkurt A, Seneca N, Tipre D, DeNucci CC, Iida H, Vaupel DB, Horti AG, Koren AO, Kimes AS, London ED, Seibyl JP, Baldwin RM, Innis RB. Quantification of nicotinic acetylcholine receptors in human brain using [123I]5-I-A-85380 SPET. Eur J Nucl Med Mol Imaging. 2003 Dec;30(12):1620-9. doi: 10.1007/s00259-003-1320-0. Epub 2003 Oct 2.
PubMed 14523584Fujita M, Ichise M, Zoghbi SS, Liow JS, Ghose S, Vines DC, Sangare J, Lu JQ, Cropley VL, Iida H, Kim KM, Cohen RM, Bara-Jimenez W, Ravina B, Innis RB. Widespread decrease of nicotinic acetylcholine receptors in Parkinson's disease. Ann Neurol. 2006 Jan;59(1):174-7. doi: 10.1002/ana.20688.
PubMed 16374823Fukuyama H. Functional brain imaging in Parkinson's disease-overview. J Neurol. 2004 Oct;251 Suppl 7:vII1-3. doi: 10.1007/s00415-004-1702-7. No abstract available.
PubMed 15505748Mamede M, Ishizu K, Ueda M, Mukai T, Iida Y, Fukuyama H, Saga T, Saji H. Quantification of human nicotinic acetylcholine receptors with 123I-5IA SPECT. J Nucl Med. 2004 Sep;45(9):1458-70.
PubMed 15347712Obrzut SL, Koren AO, Mandelkern MA, Brody AL, Hoh CK, London ED. Whole-body radiation dosimetry of 2-[18F]Fluoro-A-85380 in human PET imaging studies. Nucl Med Biol. 2005 Nov;32(8):869-74. doi: 10.1016/j.nucmedbio.2005.06.005.
PubMed 16253812
Study at a glance
From the registry record, last updated by the sponsor on 4 Jul 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Quantification of Cerebral Cholinergic Function in Patients With Parkinson´s Disease by Means of Nuclear Medicine Methods
- ClinicalTrials.gov ID
- NCT01003535
- Acronym / sponsor ID
- JoergSpiegel1
- Conditions
- Parkinson´s Disease, Acetylcholine, SPECT
- Keywords
- Parkinson´s disease, Acetylcholine receptors
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 25 participants (actual)
- Lead sponsor
- Universität des SaarlandesUniversity, hospital or other
- Study start
- Jan 2010
- Primary completion
- Apr 2012 (actual)
- Study completion
- Apr 2012 (actual)
- First posted
- 28 Oct 2009 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Parkinson´s disease is based on a Lewy body degeneration of cerebral and extracerebral neurons. This Lewy body degeneration includes cerebral cholinergic neurons besides dopaminergic neurons.
In previous studies the investigators found that some clinical parkinsonian symptoms - primarily hypokinesia and rigidity - significantly correlate with the dopaminergic nigrostriatal degeneration which was quantified by dopamine transporter imaging. In contrast to that, resting or postural parkinsonian tremor does not correlate with the dopaminergic nigrostriatal degeneration. Obviously further cerebral changes - for instance possible changes / degeneration of cerebral cholinergic neurons - contribute to parkinsonian tremor.
In this study the investigators apply cerebral 5-IA-85380-SPECT to quantify the local density of cerebral nicotinergic cholinergic receptors in patients with Parkinson´s disease. The investigators will correlate the results of cerebral 5-IA-85380-SPECT with the clinical parkinsonian main symptoms hypokinesia, rigidity and primarily resting and postural tremor. In particular, it is of interest whether changes of cerebral cholinergic neurons are involved in the generation of parkinsonian tremor.
Detailed description
The protocol of our study - as explained in the following - was approved by the Local Ethics committee (Ethics committee of the medical association of the Saarland, D-66111 Saarbrücken, Germany, file number 201/06) and by the German Federal Agency for Radiation Protection (Bundesamt für Strahlenschutz, D-38201 Salzgitter, Germany, file number Z 5 - 22461/2 2008-207).
Aims of this study:
In this study we measure the density and local distribution of cerebral acetylcholine receptors in patients with Parkinson´s disease (PD) by means of [123I]5-IA-85380 SPECT. [123I]5-IA-85380 SPECT was applied in healthy volunteers (Fujita et al. 2002, Fujita et al. 2003, Ding et al. 2004, Mamede et al. 2004, Obrzut et al. 2005) and PD patients (Fukuyama et al. 2004, Bucerius et al. 2006, Fujita et al. 2006). These numerous previous studies proved that [123I]5-IA-85380 SPECT is a safe and effective method to visualize cerebral acetylcholine receptors.
We intend to correlate the density and distribution of cerebral acetylcholine receptors with the clinical parkinsonian cardinal symptoms tremor, hypokinesia and rigidity. The patients are out-patients who are treated by the Department of Neurology, Saarland University, D-66421 Homburg/Saar, Germany. The nuclear medicine measurement [123I]5-IA-85380 SPECT will be performed in the Department of Nuclear medicine of the University of Würzburg, D-97080 Würzburg, Germany.
This study should answer the following questions:
- Does the density of acetylcholine receptors in putamen, caudate nucleus, thalamus and pons correlate with the severity of the clinical symptoms hypokinesia, rigidity, resting tremor, postural tremor?
- Do PD patients with the tremor dominant type, akinetic rigid type and equivalence type differ concerning their accumulation of 5-IA-85380 (=density of acetylcholine receptors) in the putamen, caudate nucleus, thalamus and pons?
Study protocol:
This study will include 25 patients with Parkinson´s disease (PD), Hoehn and Yahr stage 1. 25 patients have to be included ,if a correlation coefficient r = 0.5, an error 1st order = 0.05 and an error 2nd order = 0.20 are assumed. In addition, the number of 25 patients was sufficient in previous studies to obtain significant results. Due to the stochastic risk of radiation-induced long-term side effects (for example neoplasms), which is higher in younger patients, the lower age limit of included patients is determined to 50 years. The upper age limit is 75 years, since vascular cerebral changes increase exponentially in the higher age. The antiparkinsonian medication - except anticholinergic medication - can be continued during the nuclear medicine examination because previous studies excluded any interference between antiparkinsonian medication - except anticholinergic medication - and 5-IA-85380 SPECT.
The severity of the clinical parkinsonian motor symptoms hypokinesia, rigidity, resting tremor and postural tremor are quantified by means of the motor part of the UPDRS (Unified Parkinson´s Disease Rating Scale). The UPDRS is measured in the "Off"-state; "Off"-state means that the medication was interrupted for at least twelve hours. Further the Mini Mental State-Test and DemTect are measured. Healthy controls are not included since there exist norm values in the literature (Fujita et al. 2002, Fujita et al. 2003, Ding et al. 2004, Mamede et al. 2004, Obrzut et al. 2005).
The tracer [123I]5-IA-85380 is produced in the laboratory of radiochemistry and radiopharmacy of the University of Würzburg at the day of examination. This laboratory has the official permission to produce radiotracers. After informed consent by the patient and thyroid gland blocking with perchlorate, the radioactively marked tracer [123I]5-IA-85380 (185 MBq) was given intravenously. Cerebral SPECT imaging was performed 2-3 hours after intravenous injection of the radioactive substance [123I]5-IA-85380. A triple-head gamma camera equipped with low-energy high-resolution collimators was used. Data was acquired in a 128 x 128 matrix covering 120 degrees per camera and head, 50 seconds per view. A total of 120 views was acquired.
Statistical analysis:
The correlation between density of acetylcholine receptors (= uptake of [123I]5-IA-85380) in different brain regions is correlated with the severity of clinical symptoms. The latter was quantified by the items of the UPDRS score.
Correlations were calculated using the Pearson´s correlation coefficient in case of a normally distributed data and Spearman´s correlation coefficient in case of a not normally distributed data.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| [123I]5-IA-85380 SPECT | – | – |
Who may qualify
- Ages
- 50 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with Parkinson´s disease
Key inclusion criteria (5 listed)
- patients with Parkinson´s disease (after the UK Brain Bank criteria)
- Hoehn and Yahr stage 1
- age 50 - 75 years
- non-smokers
- informed consent to participate in the study
Key exclusion criteria (9 listed)
- pregnant or nursing women
- no adequate contraception in women who are capable of childbearing
- male patients living with fertile women without adequate contraception
- smokers
- actual or past drug or alcohol abuse
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Correlation of density of acetylcholine receptors in distinct brain areas versus the clinical parameters resting tremor, postural tremor, hypokinesia and rigidity in patients with Parkinson´s disease
Time frame: 1 time
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Jul 2012.
- Background: PubMed 16598519Bucerius J, Joe AY, Schmaljohann J, Gundisch D, Minnerop M, Biersack HJ, Wullner U, Reinhardt MJ. Feasibility of 2-deoxy-2-[18F]fluoro-D-glucose- A85380-PET for imaging of human cardiac nicotinic acetylcholine receptors in vivo. Clin Res Cardiol. 2006 Feb;95(2):105-9. doi: 10.1007/s00392-006-0342-6. Epub 2006 Jan 19.
- Background: PubMed 15236351Ding YS, Fowler JS, Logan J, Wang GJ, Telang F, Garza V, Biegon A, Pareto D, Rooney W, Shea C, Alexoff D, Volkow ND, Vocci F. 6-[18F]Fluoro-A-85380, a new PET tracer for the nicotinic acetylcholine receptor: studies in the human brain and in vivo demonstration of specific binding in white matter. Synapse. 2004 Sep 1;53(3):184-9. doi: 10.1002/syn.20051. No abstract available.
- Background: PubMed 11926380Fujita M, Seibyl JP, Vaupel DB, Tamagnan G, Early M, Zoghbi SS, Baldwin RM, Horti AG, KoreN AO, Mukhin AG, Khan S, Bozkurt A, Kimes AS, London ED, Innis RB. Whole-body biodistribution, radiation absorbed dose, and brain SPET imaging with [123i]5-i-A-85380 in healthy human subjects. Eur J Nucl Med Mol Imaging. 2002 Feb;29(2):183-90. doi: 10.1007/s00259-001-0695-z.
- Background: PubMed 14523584Fujita M, Ichise M, van Dyck CH, Zoghbi SS, Tamagnan G, Mukhin AG, Bozkurt A, Seneca N, Tipre D, DeNucci CC, Iida H, Vaupel DB, Horti AG, Koren AO, Kimes AS, London ED, Seibyl JP, Baldwin RM, Innis RB. Quantification of nicotinic acetylcholine receptors in human brain using [123I]5-I-A-85380 SPET. Eur J Nucl Med Mol Imaging. 2003 Dec;30(12):1620-9. doi: 10.1007/s00259-003-1320-0. Epub 2003 Oct 2.
- Background: PubMed 16374823Fujita M, Ichise M, Zoghbi SS, Liow JS, Ghose S, Vines DC, Sangare J, Lu JQ, Cropley VL, Iida H, Kim KM, Cohen RM, Bara-Jimenez W, Ravina B, Innis RB. Widespread decrease of nicotinic acetylcholine receptors in Parkinson's disease. Ann Neurol. 2006 Jan;59(1):174-7. doi: 10.1002/ana.20688.
- Background: PubMed 15505748Fukuyama H. Functional brain imaging in Parkinson's disease-overview. J Neurol. 2004 Oct;251 Suppl 7:vII1-3. doi: 10.1007/s00415-004-1702-7. No abstract available.
- Background: PubMed 15347712Mamede M, Ishizu K, Ueda M, Mukai T, Iida Y, Fukuyama H, Saga T, Saji H. Quantification of human nicotinic acetylcholine receptors with 123I-5IA SPECT. J Nucl Med. 2004 Sep;45(9):1458-70.
- Background: PubMed 16253812Obrzut SL, Koren AO, Mandelkern MA, Brody AL, Hoh CK, London ED. Whole-body radiation dosimetry of 2-[18F]Fluoro-A-85380 in human PET imaging studies. Nucl Med Biol. 2005 Nov;32(8):869-74. doi: 10.1016/j.nucmedbio.2005.06.005.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Joerg Spiegel, M.D. principal investigator
Department of Neurology, Saarland University, Kirrberger Strasse, D-66421 Homburg/Saar, Germany
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Parkinson´s Disease and Acetylcholine, run by Universität des Saarlandes at 1 site in Germany.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Jul 2012. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Correlation of density of acetylcholine receptors in distinct brain areas versus the clinical parameters resting tremor, postural tremor, hypokinesia and rigidity in patients with Parkinson´s disease (time frame: 1 time). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01003535, which also lists 8 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Jul 2012.