Meta AnalysisID 7717
精氨酸治疗镰状细胞病血管闭塞危象疼痛管理：一项系统评价
CRD42023399433
Is arginine beneficial for pain management in sickle cell disease during vaso-occlusive crisis compared to placebo?
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Record Fields
Scalar fields from the final meta_analysis record.
- Meta Analysis Id
- 7717
- Evidence Id
- 16275
- Core Evidence Id
- 16275
- Source Meta Analysis Id
- 7712
- Herb2 Meta Analysis Id
- HBMA007712
- Crd Id
- CRD42023399433
- Title
- Arginine therapy for pain management in sickle cell disease during vaso-occlusive crisis : A systematic review
- Review Question
- Is arginine beneficial for pain management in sickle cell disease during vaso-occlusive crisis compared to placebo?
- Study Type Included
- Randomized controlled trials and clinical trials
- Condition Being Studied
- Sickle cell disease (SCD) is a group of inherited red blood cell disorders. A vaso-occlusive crisis, or VOC, occurs when sickled red blood cells block blood flow to the point that tissues become deprived of oxygen.
- Participant
- Sickle cell patients with vaso-occlusive crisis
- Animal
- Human Disease Modelled
- Intervention
- Arginine administration
- Comparator Control
- Placebo
- Main Outcome
- Efficacy of Arginine in pain management during vaso-occlusive crises
- Outcome Measure
- Additional Outcome
- Study Method
- Systematic review
- Keyword
- Anemia, Sickle Cell; Arginine; Hemoglobinopathies; Humans; Pain Management
- Contact
- ahmed gatea [email protected]
- Organisational Affiliation
- Negida academy
- Funding Source
- Nigeda academy, Arlington, MA
- Other Selection Criteria
- Final Publication
- Same Topic Review
- Published Protocol
- Review Type
- Language
- English
- Country
- Egypt, Iraq
- Review Stage
- Review Ongoing
- First Submission Date
- 2023-02-19
- Registration Date
- 2023-03-02
- Anticipated Start Date
- 2023-02-14
- Anticipated Completion Date
- 2023-04-30
- Title Cn
- 精氨酸治疗镰状细胞病血管闭塞危象疼痛管理：一项系统评价
- Title En
- Arginine therapy for pain management in sickle cell disease during vaso-occlusive crisis : A systematic review
- Bilingual Status
- complete