- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02917070
Parental Consanguinity and Family History of Kidney Disease in Turkish Kidney Disease Population (CAKD)
September 26, 2016 updated by: Yasar Caliskan, Istanbul University
The Importance of Parental Consanguinity and Family History of Kidney Disease in Turkish Adult Chronic Kidney Disease Population
Inbreeding and consanguineous marriages are known to increase the risk of autosomal recessive disorders.
The aim of this study was to examine the association between consanguinity and kidney diseases in the adult Turkish population.
Study Overview
Detailed Description
This was a national, cross-sectional study recruiting patients from nephrology out-patient clinics and dialysis units.
All patients between 18 and 70 years of age who were on follow up in outpatient clinic and dialysis unit at the Istanbul Medical Faculty from October 2009 to October 2015 were included in the study.
All patients and healthy controls enrolled in this study gave informed consent to participate in the survey.
They were all asked to answer a questionnaire including socio-demographic data, history of familial kidney disease and consanguineous marriage.
Additional information was obtained from their private physicians and medical files.
To ensure reliability of administration of the questionnaire, all interviewers underwent training using a standardized protocol.
Study Type
Observational
Enrollment (Actual)
2576
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Istanbul, Turkey, 34030
- Istanbul University, Istanbul Faculty of Medicine
-
-
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
18 years to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All patients between 18 and 70 years of age who were on follow up in outpatient clinic and dialysis unit at the Istanbul Medical Faculty from October 2009 to October 2015 were included in the study
Description
Inclusion Criteria:
- follow up in outpatient clinic and dialysis unit at the Istanbul Medical Faculty
- between 18-70 years old
- provide informed consent
Exclusion Criteria:
- follow-up shorter than 6 months
- patients whose data were not available
- patients who were unwilling or unable to provide informed consent
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy controls
Healthy subjects
|
|
|
Patients
Patients who have chronic kidney diseases
|
In this study we aimed to investigate effect of family history and consanguineous marriage in the development of CKD in the adult Turkish population.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Effect of parental consanguinity on chronic kidney disease confirmed by a questionnaire did they have consanguinity marriage or not.
Time Frame: 6 months after enrollment
|
6 months after enrollment
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Effect of family history of kidney disease on the development of chronic kidney confirmed by a questionnaire did they have any parents with chronic kidney diseases or not.
Time Frame: 6 months after enrollment
|
6 months after enrollment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yasar Caliskan, Dr., Istanbul University, Istanbul Faculty of Medicine, Department of Internal Medicine, Division of Nephrology
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- National Kidney Foundation. K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification. Am J Kidney Dis. 2002 Feb;39(2 Suppl 1):S1-266. No abstract available.
- Chronic Kidney Disease Prognosis Consortium; Matsushita K, van der Velde M, Astor BC, Woodward M, Levey AS, de Jong PE, Coresh J, Gansevoort RT. Association of estimated glomerular filtration rate and albuminuria with all-cause and cardiovascular mortality in general population cohorts: a collaborative meta-analysis. Lancet. 2010 Jun 12;375(9731):2073-81. doi: 10.1016/S0140-6736(10)60674-5. Epub 2010 May 17.
- Suleymanlar G, Utas C, Arinsoy T, Ates K, Altun B, Altiparmak MR, Ecder T, Yilmaz ME, Camsari T, Basci A, Odabas AR, Serdengecti K. A population-based survey of Chronic REnal Disease In Turkey--the CREDIT study. Nephrol Dial Transplant. 2011 Jun;26(6):1862-71. doi: 10.1093/ndt/gfq656. Epub 2010 Nov 4.
- Gumprecht J, Zychma MJ, Grzeszczak W, Zukowska-Szczechowska E; End-stage Renal Disease Study Group. Human SA gene Pst1 polymorphism and chronic renal failure: results of the family-based study. Nephrol Dial Transplant. 2001 Feb;16(2):387-90. doi: 10.1093/ndt/16.2.387.
- O'Dea DF, Murphy SW, Hefferton D, Parfrey PS. Higher risk for renal failure in first-degree relatives of white patients with end-stage renal disease: a population-based study. Am J Kidney Dis. 1998 Nov;32(5):794-801. doi: 10.1016/s0272-6386(98)70135-0.
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
February 1, 2016
Primary Completion (Actual)
May 1, 2016
Study Completion (Actual)
August 1, 2016
Study Registration Dates
First Submitted
September 9, 2016
First Submitted That Met QC Criteria
September 26, 2016
First Posted (Estimate)
September 28, 2016
Study Record Updates
Last Update Posted (Estimate)
September 28, 2016
Last Update Submitted That Met QC Criteria
September 26, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2016/257
- 301 (Yasar Calıskan)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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.
Clinical Trials on Hereditary Diseases
-
Columbia UniversityNatera, Inc.RecruitingHereditary Cancer SyndromeUnited States
-
Pharvaris Netherlands B.V.Enrolling by invitationHereditary Angioedema | Hereditary Angioedema Type I | Hereditary Angioedema Type II | Hereditary Angioedema Types I and II | Hereditary Angioedema Attack | Hereditary Angioedema With C1 Esterase Inhibitor Deficiency | Hereditary Angioedema - Type 1 | Hereditary Angioedema - Type 2 | C1 Esterase Inhibitor... and other conditionsUnited States, Austria, Spain, Australia, Italy, United Kingdom, Bulgaria, France, Germany, Hungary, Israel, Argentina, Canada, Czechia, Hong Kong, Japan, Netherlands, Puerto Rico, South Africa, Sweden, Brazil, Poland, Saudi Arabia, South... and more
-
National Cancer Centre, SingaporeCompletedHereditary Cancer SyndromesSingapore
-
Pharvaris Netherlands B.V.CompletedHereditary Angioedema | Hereditary Angioedema Type I | Hereditary Angioedema Type II | Hereditary Angioedema Types I and II | Hereditary Angioedema Attack | Hereditary Angioedema With C1 Esterase Inhibitor Deficiency | Hereditary Angioedema - Type 1 | Hereditary Angioedema - Type 2 | C1 Esterase Inhibitor... and other conditionsBulgaria, United States, Spain, Israel, Germany, Poland, Canada, Czechia, France, Hungary, Italy, Netherlands, United Kingdom
-
Pharvaris Netherlands B.V.CompletedHereditary Angioedema | Hereditary Angioedema Type I | Hereditary Angioedema Type II | Hereditary Angioedema Types I and II | Hereditary Angioedema Attack | Hereditary Angioedema With C1 Esterase Inhibitor Deficiency | Hereditary Angioedema - Type 1 | Hereditary Angioedema - Type 2 | C1 Esterase Inhibitor... and other conditionsUnited States, Austria, Australia, Italy, Spain, United Kingdom, Netherlands, Bulgaria, Germany, Hungary, Argentina, Canada, Czechia, France, Hong Kong, Japan, South Africa, Sweden, Brazil, Poland, Saudi Arabia, South Korea, Turkey... and more
-
Pharvaris Netherlands B.V.CompletedHereditary Angioedema | Hereditary Angioedema Type I | Hereditary Angioedema Type II | Hereditary Angioedema Types I and II | Hereditary Angioedema Attack | Hereditary Angioedema With C1 Esterase Inhibitor Deficiency | Hereditary Angioedema - Type 1 | Hereditary Angioedema - Type 2 | C1 Esterase Inhibitor... and other conditionsUnited States, Poland, Germany, Austria, Bulgaria, Canada, Ireland, Italy, United Kingdom
-
ADARx Pharmaceuticals, Inc.RecruitingHereditary Angioedema - Type 1 | Hereditary Angioedema - Type 2 | Hereditary Angioedema (HAE) | HAEUnited States, Argentina, Australia, Belgium, Canada, China, France, Germany, Hong Kong, Israel, Austria, Bulgaria, Croatia, Czechia, Hungary, Poland, Spain, Taiwan, United Kingdom
-
University Hospital, AngersNot yet recruitingMitochondrial Disease | Leber's Hereditary Optic Neuropathy (LHON) | Leber Hereditary Optic Neuropathy (LHON) | Optic Nerve DiseaseFrance
-
GenSight BiologicsRecruitingLeber Hereditary Optic DiseaseFrance
-
University of UtahUniversity of Witwatersrand, South AfricaCompletedHereditary Elliptocytosis (HE) | Hereditary Pyropoikilocytosis (HPP)United States
Clinical Trials on Patients
-
Sheba Medical CenterRecruitingMental Health DiagnosisIsrael
-
IRCCS Centro Neurolesi "Bonino-Pulejo"RecruitingDementia | Mild Cognitive ImpairmentItaly
-
IRCCS Ospedale San RaffaeleMinistero della Salute, Italy; Azienda Ospedaliera OO.RR. S. Giovanni di Dio... and other collaboratorsRecruitingCrohn Disease | Ulcerative ColitisItaly
-
Federal Center of Cerebrovascular Pathology and...Moscow Technical University of Communications and InformaticsNot yet recruitingStroke | Hemiparesis | Spasticity as Sequela of Stroke | Dysmetria
-
Unity Health TorontoActive, not recruiting
-
The First Affiliated Hospital of Zhengzhou UniversityRecruiting
-
G. d'Annunzio UniversityCompleted
-
University Hospital, RouenCompleted
-
Yonsei UniversityCompletedMedical StudentsKorea, Republic of
-
Eastern Mediterranean UniversityCompletedObesity | Bariatric Surgery Candidate | Healthy Eating IndexCyprus