Screening of Congenital Anomalies of Kidney

NCT ID: NCT06440499

Last Updated: 2024-06-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

250 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-07-01

Study Completion Date

2025-04-05

Brief Summary

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To evaluate the role of ultrasound in prenatal diagnosis of congenital anomalies of kidney and urinary system in third trimester of pregnancy.

Primay outcomes:

To determine incidence of congenital anomalies in kidney and urinary system in Third Timerter by ultrasound.

Detailed Description

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Conditions

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Kidney Congenital Anomalies

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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US

Us

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* • Singleton pregnancy.

* Healthy women Aged between 20 to 40 years old.
* Third trimester

Exclusion Criteria

* • Multiples pregnancies.

* Maternal D.M or HTN
* Patients\' refusal to participate.
Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Mohamed Salah

Assiut University

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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[email protected] screening of congenital anomalies of kidney

Role: CONTACT

201065574768

References

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Al-Hamed MH, Sayer JA, Alsahan N, Tulbah M, Kurdi W, Ambusaidi Q, Ali W, Imtiaz F. Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families. J Nephrol. 2021 Jun;34(3):893-900. doi: 10.1007/s40620-020-00795-0. Epub 2020 Jul 8.

Reference Type BACKGROUND
PMID: 32643034 (View on PubMed)

Other Identifiers

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congenital anomalies of kidney

Identifier Type: -

Identifier Source: org_study_id

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