RecruitingNot applicableNCT07174440
Contrast and Anesthetic Level With Lumbar Erector Spinae Plan (ESP) Block
Studying Infantile neuroaxonal dystrophy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University Hospitals Cleveland Medical Center
- Principal Investigator
- Salim Hayek, MDUniversity Hospitals Cleveland Medical Center
- Intervention
- Ropivacaine (Epidural analgesia)(drug)
- Enrollment
- 32 enrolled
- Eligibility
- 21-75 years · All sexes
- Timeline
- 2025 – 2027
Study locations (1)
- University Hospitals Cleveland Medical Center, Cleveland, Ohio, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT07174440 on ClinicalTrials.govOther trials for Infantile neuroaxonal dystrophy
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