Pattern of AFP in Chhidren Admitted at Sohag University Hospital
NCT07775066 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 30
Last updated 2026-08-20
Summary
This study is observational study aims to study the Clinical profile, Possible risk factors and Outcome of Acute flaccid paralysis in children at Sohag University Hospital.
Our study will include all children admitted to pediatric emergency and intensive care units with claim or suspicion to have acute falccid paralysis
Conditions
- Acute Flaccid Paralysis
- AFP
- Gullian Barre Syndrome
- Transverse Myelitis
Interventions
- OTHER
-
Observitional follow-up
No expiremental intervention. Data will be collected from routine cinical care, medical records and folow up visits according to standard hospital protocols
Sponsors & Collaborators
-
Mohamed Aboelhamd Ali
lead OTHER
Eligibility
- Min Age
- 1 Month
- Max Age
- 16 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-08-01
- Primary Completion
- 2027-08-01
- Completion
- 2027-09-01
Countries
- Egypt
Study Locations
More Related Trials
-
Trehalose Administration in Subjects With Spastic Paraplegia 11 (3AL-SPG11)
NCT04912609 ·Status: COMPLETED
-
Pro-inflammatory Cytokines in Facioscapulohumeral Muscular Dystrophy (CYTOKINE-FSH)
NCT04694456 ·Status: COMPLETED ·Phase: NA
-
Clinical, Genetic and Epigenetic Characterization of Patients With FSHD Type 1 and FSHD Type 2
NCT01970735 ·Status: COMPLETED ·Phase: NA
-
HEmiplegia Arrhythmia Retrospective Trial
NCT04944927 ·Status: COMPLETED
-
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia
NCT04712812 ·Status: RECRUITING
-
FSHD Molecular Characterization
NCT06096441 ·Status: TERMINATED
-
ADVANCED FSHD-COM: New Clinical Outcome Measures to Evaluate Non-ambulant FSHD Patients, a Pilot Study
NCT05453461 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Natural History Study of Oculopharyngeal Muscular Dystrophy
NCT03161847 ·Status: WITHDRAWN
-
Muscle Abnormalities in Children With XLH
NCT05312086 ·Status: UNKNOWN ·Phase: NA
-
Prospective Follow-up of Patients With Glycogen Storage Disease Type III
NCT01563705 ·Status: UNKNOWN ·Phase: NA
-
Effect of Captopril on GLS in Duchenne Myodystrophy
NCT06485661 ·Status: RECRUITING ·Phase: EARLY_PHASE1
-
Stroke in Young Fabry Patients (sifap2): Characterization of the Stroke Rehabilitation
NCT00413595 ·Status: COMPLETED
-
1 Year MRI Followup in Facioscapulohumeral Muscular Dystrophy
NCT02159612 ·Status: COMPLETED
-
A Long Term Follow-Up Study of Fabry Disease Subjects Treated With FLT190
NCT04455230 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Facioscapulohumeral Dystrophy in Children
NCT02625662 ·Status: COMPLETED
-
Natural History of Oculo-Pharyngeal Muscular Dystrophy (OPMD) - Israel National OPMD Registry
NCT07146256 ·Status: RECRUITING
-
Study Determining the Frequency of Duchenne Muscular Dystrophy and Late-onset Pompe Disease
NCT04120168 ·Status: COMPLETED
-
Study of the Causes of the Breakdown of Muscle Fibers in Hospitalized Patients
NCT01022450 ·Status: UNKNOWN
-
Predictors and Prognostic Factors of Gullian Barrie Syndrome Outcome
NCT04927598 ·Status: COMPLETED
-
Liver and the Spleen Stifness in Adult Patients With Gaucher's Disease Using Ultrasound Shear Wave Elastography
NCT03896607 ·Status: TERMINATED
-
Study of the Spermatic Characteristics of Patients With Fabry Disease
NCT04073888 ·Status: TERMINATED ·Phase: NA
-
Validation of a Clinical Assessment Scale Specific to Alternating Hemiplegia
NCT06007521 ·Status: COMPLETED
-
Pathology Analysis of OPMD Patient Myotomies
NCT03874910 ·Status: UNKNOWN
-
National Registry for Egyptian Pediatric Neuromuscular Diseases
NCT02124616 ·Status: UNKNOWN
-
A Global Prospective Observational Study of Women With Fabry Disease and Their Infants During Pregnancy and Breastfeeding
NCT04252066 ·Status: RECRUITING