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General ParesisNCT00921648

Clinical Findings in General Paresis

An observational study of General Paresis, run by Xijing Hospital at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This is a study of the clinical and neuroimaging of general paresis. The investigators studied six patients with general paresis. Read more about this study

Who is it for?
Ages 30 to 60 years
Conditions the study is for
General Paresis
How many people
6 participants
Where
1 siteChina
Study dates
Apr 2008to Jan 2009
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 30 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Study population: 6 cases

Who may be able to join

  • EEG MR

Who cannot join

  • Serological test

Trial locations and contacts

1 site in 1 country.

China1 site
  • Xijing Hospital

    Xi'an, Shaanxi, 710032

Other trials in China

About this study

Official title: Xijing HOSPITAL, Fourth Military Medical University, China

This is a study of the clinical and neuroimaging of general paresis. The investigators studied six patients with general paresis.

Read the detailed description

Inclusion Criteria:

  • Mental disorders
  • positive TPHA in CSF and sera
  • HIV-negative serology by ELISA

Exclusion Criteria:

  • Negative TPHA in CSF and sera
  • No image data
Conditions
General Paresis
Keywords
EEG, general paresis, MRI, neurosyphilis
Medical subject headings
Neurosyphilis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT00921648
Study groupRoleWhat they receive
Mr Q, 40 years oldDementia, sensory aphasia, irritability, hallucination MRI showed cortical lesion, mesial temporal lobe atrophy.
Mr Guo,35 years oldDementia, sensory aphasia, tremor, gait disturbance MRI showed cortical lesion, enlarged ventricle, white matter lesion, cerebral atrophy
Mr Zhang,40 years oldDementia, apraxia of speech, gatism , irritability, insomnia, gait disturbance MRI showed white matter lesion, cerebral atrophy.
Mr Liu,40 years oldDementia, apraxia of speech, irritability, insomnia MRI showed normal.
Mr Zhang,54 years oldDementia, apraxia of speech MRI showed white matter lesion, cerebral atrophy.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Jun 2009 (estimated)
  2. Study startApr 2008
  3. Primary completionDec 2008
  4. Study completionJan 2009

Resources

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
Case only
Time perspective
Retrospective
Enrolment
6 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00921648
Sponsor's protocol ID
20080301
Status last verified
Jun 2009
First submitted
21 Oct 2008
Last updated
16 Jun 2009
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of General Paresis, run by Xijing Hospital at 1 site in China.

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 1 inclusion and 1 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 16 Jun 2009. 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 China. 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.

Where can I read the original study information?
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 16 Jun 2009.

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