A Real-World Medical Chart Review of Spinal Muscular Atrophy Patients Treated With Onasemnogene Abeparvovec in Saudi Arabia (SMA-REAL)
Spinal Muscular Atrophy Center-based REAL World Retrospective Medical Chart Review of Patient Treated With Onasemnogene Abeparvovec (Zolgensma®) in Saudi Arabia
연구 개요
상태
상태
정황
정황
연구 유형
연구 유형
등록 (추정된)
등록
연락처 및 위치
연구 연락처
연구 연락처
- 이름: Novartis Pharmaceuticals
- 전화번호: +41613241111
- 이메일: novartis.email@novartis.com
연구 연락처 백업
- 이름: Novartis Pharmaceuticals
참여기준
자격 기준
자격 기준
공부할 수 있는 나이
- 어린이
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
Inclusion criteria:
- Patients with a genetically confirmed diagnosis of SMA type 1 who were treated with OA.
- Availability of data on at least one visit before treatment initiation and two visits post-treatment is a must for inclusion.
- Patients who were treated with OA starting in January 2023.
- Patients with at least 3 months of follow-up following the treatment with OA.
Exclusion criteria:
1. Any patient who does not fulfill any of the inclusion criteria listed above.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
그룹/코호트 수
코호트 및 개입
그룹/코호트그룹/코호트 |
|---|
|
OA Cohort
Patients with SMA type 1 who were treated with OA.
|
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Proportion of SMA Type 1 Non-Sitters Patients Achieving Independent Sitting for ≥30 Seconds at Any Visit up to 12 Months After OA Administration
기간: Up to 12 months
|
Up to 12 months
|
2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP-INTEND) Score
기간: Up to approximately 3 years
|
CHOP-INTEND is a validated motor function assessment for infants with SMA.
The total score ranges from 0 to 64, with higher scores indicating better motor function.
Scores are derived from 16 items assessing spontaneous movement, strength, and motor abilities.
An increase in score reflects improvement in motor function.
|
Up to approximately 3 years
|
|
Change From Baseline in CHOP-INTEND Score
기간: Baseline, up to approximately 3 years
|
CHOP-INTEND is a validated motor function assessment for infants with SMA.
The total score ranges from 0 to 64, with higher scores indicating better motor function.
Scores are derived from 16 items assessing spontaneous movement, strength, and motor abilities.
An increase in score reflects improvement in motor function.
|
Baseline, up to approximately 3 years
|
|
Hammersmith Infant Neurological Examination-Section 2 (HINE-2, Motor Milestones) Score
기간: Up to approximately 3 years
|
The HINE-2 is a motor milestone assessment evaluating developmental abilities in infants.
The total score ranges from 0 to 26, with higher scores indicating greater achievement of motor milestones.
The scale assesses milestones such as head control, sitting, rolling, crawling, standing, and walking.
Higher scores correspond to more advanced motor development.
|
Up to approximately 3 years
|
|
Change From Baseline in HINE-2 Score
기간: Baseline, up to approximately 3 years
|
The HINE-2 is a motor milestone assessment evaluating developmental abilities in infants.
The total score ranges from 0 to 26, with higher scores indicating greater achievement of motor milestones.
The scale assesses milestones such as head control, sitting, rolling, crawling, standing, and walking.
Higher scores correspond to more advanced motor development.
|
Baseline, up to approximately 3 years
|
|
Percentage of Patients who Maintain the Ability to Thrive at 12 Months After OA Treatment
기간: 12 months
|
Ability to thrive is defined as meeting the following criteria:
|
12 months
|
|
Number and Percentage of Patients Without Permanent Ventilatory Support or Death After OA Administration
기간: Up to approximately 3 years
|
Event-free survival of patients without permanent ventilatory support or death after OA administration. Permanent ventilatory support is defined as the requirement for either:
|
Up to approximately 3 years
|
|
Number and Percentage of Patients With Adverse Events
기간: Up to approximately 3 years
|
Up to approximately 3 years
|
|
|
Number and Percentage of Patients by Demographic and Clinical Characteristics
기간: Baseline
|
Demographic and clinical characteristics include:
|
Baseline
|
|
Age
기간: Baseline
|
Age, gestational age at birth, age at symptom onset, and age at SMA type 1 diagnosis.
|
Baseline
|
|
Duration Between Symptom Onset and Diagnosis
기간: Baseline
|
Baseline
|
공동 작업자 및 조사자
수사관
수사관
- 연구 책임자: Novartis Pharmaceuticals, Novartis Pharmaceuticals
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- COAV101A1SA01
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .