- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04386889
SLE Vasculitis In Egyptian Patients
December 11, 2020 updated by: Prof. Dr. /Tayseer Abdulaal, Tabarak New Cairo Hospital (TNCH)
SLE Vasculitis Incidence In Female Egyptian Patients
Systemic lupus erythematosus (SLE) is a complex heterogeneous autoimmune disease with a wide variety of clinical and serological manifestations that may affect any organ.
Vasculitis prevalence in SLE is reported to be between 11% and 36%.
Study Overview
Detailed Description
Systemic lupus erythematosus (SLE) is a complex heterogeneous autoimmune disease with a wide variety of clinical and serological manifestations that may affect any organ.
Vasculitis prevalence in SLE is reported to be between 11% and 36%.
A diverse clinical spectrum, due to inflammatory involvement of vessels of all sizes, is present.
Even though cutaneous lesions, representing small vessel involvement, are the most frequent, medium and large vessel vasculitis may present with visceral affection, with life-threatening manifestations such as mesenteric vasculitis, pulmonary hemorrhage, or mononeuritis multiplex, with detrimental consequences.
Early recognition and an appropriate treatment are crucial.
Recent studies have shown that vasculitis in patients with SLE may present different clinical forms based on the organ involved and the size of the affected vessel.
It is noteworthy that the episodes of vasculitis are not always accompanied by high disease activity.
Recent articles on this topic have focused on new treatments for the control of vascular disease, such as biological therapies such as Rituximab and Belimumab, among others.
Study Type
Interventional
Enrollment (Anticipated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Tayseer A Abdulaal, M.D.
- Phone Number: +201223407675
- Email: tayseer@mail.com
Study Locations
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-
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Cairo, Egypt, 11613
- Recruiting
- Tabarak New Cairo Hospital
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Contact:
- Tayseer A Abdulaal, M.D.
- Phone Number: +201223407675
- Email: tayseer@mail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
22 years to 45 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- LE or suspected SLE established by ACR criteria
- Ability to give informed consent
- Adult and minor relatives (first and second degree) of individuals Included in IV-G (only for genetic studies)
- Ability of the patient or minor relative s parents to give informed consent
- Affected individuals age greater than or equal to 9 years with no upper age limit
- Healthy Volunteers (non-related) age greater than or equal to 18 with no upper age limit
- Healthy Volunteers (first- and second-degree relatives) age greater than or equal to 9 with no upper age limit
- Vascular studies adults only age greater than or equal to 18 with no upper age limit
Exclusion Criteria:
- Concomitant medical problems which would confound the interpretation of studies gathered by this protocol. Included in this is the presence of HIV in the blood, active malignancies, or other significant medical conditions that may interferes with interpretation of some lupus studies.
- Concomitant medical, surgical or other conditions for which inadequate facilities are available to support their care at NIH.
Inability or unwillingness to comply with follow up requirements (e.g. distance, social, physical limitations)
- Any comorbidity of medical or psychological/psychiatric condition or treatment after reviewing of patients previous or outside medical records, that in the opinion of the Principal Investigator, would exclude the subjects from the research studies (e.g. Patient requiring urgent and/or acute medical care, surgical or other procedures)
- Unwilling to participate in research studies or to provide research samples or data.
Criteria for exclusion:
- Any concomitant medical problems or are taking medications which would confound the interpretation of studies they are considered for
EXCLUSION CRITERIA FOR VASCULAR STUDIES ONLY, FOR SLE AND HEALTHY CONTROLS:
- Subjects with a contraindication to MRI scanning will not receive the optional Cardiovascular MRI. These contraindications include subjects with the following devices:
- Central nervous system aneurysm clips unless it is labeled safe or conditional for MRI
- Implanted neural stimulator (e.g.TENS-Unit) unless it is labeled safe or conditional for MRI
- Implanted cardiac pacemaker or defibrillator
- Cochlearor any type of ear implant unless it is labeled safe or conditional for MRI
- Ocular foreign body (e.g. metal shavings)
- Implanted Insulin pump or drug infusion device unless it is labeled safe or conditional for MRI
- Metal shrapnel or bullet unless cleared by plain x-ray as safe for MRI
- Subjects with renal excretory dysfunction, estimated glomerular filtration rate < 60 mL/min/1.73m(2) using the CKD-EPI equation or equivalent (using the CRIS-calculated eGFR to define the threshold) and a serum creatinine measured within 2 weeks without intercurrent change in medical condition or medications. Subjects meeting this exclusion criterion may still be included in the study but will not be exposed to the cardiac CT angiography, or gadolinium-based contrast agents.
- Any clinical instability precluding subject from getting MRI as determined by the enrolling clinician.
- Pregnant or lactating women will be excluded from vascular studies.
- Healthy controls with known history of coronary artery disease, peripheral vascular disease or atherosclerosis.
- Individuals younger than 18 years old will be excluded given the radiation exposure as well as the lack of proper validation for the proposed vascular function studies.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: SLE Vasculitis
20 SLE Female patients will subjected to study of the all vasculitic pattern that may occur.
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20 SLE female Egyptian patients, among them we are going to study the vasculitic pattern incidence.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
SLE Vasculitis
Time Frame: 6 months
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Incidence of vasculitic pattern
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6 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
March 25, 2021
Primary Completion (Anticipated)
July 25, 2021
Study Completion (Anticipated)
August 25, 2021
Study Registration Dates
First Submitted
May 9, 2020
First Submitted That Met QC Criteria
May 12, 2020
First Posted (Actual)
May 13, 2020
Study Record Updates
Last Update Posted (Actual)
December 14, 2020
Last Update Submitted That Met QC Criteria
December 11, 2020
Last Verified
December 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SLE Tabarak 01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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