RecruitingPhase 3NCT06593665
Intrathecal Morphine Versus Intravenous Methadone for Postoperative Analgesia Following Retroperitoneal Lymph Node Dissection.
Studying Tumor of testis and paratestis
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
- Indiana University
- Principal Investigator
- Gulraj S Chawla, MDIndiana University
- Intervention
- Inrathecal Morphine(drug)
- Enrollment
- 142 target
- Eligibility
- 18-80 years · MALE
- Timeline
- 2024 – 2026
Study locations (2)
- Indiana Univeristy, Indianapolis, Indiana, United States
- Indiana University Hospital, Indianapolis, Indiana, 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 NCT06593665 on ClinicalTrials.govOther trials for Tumor of testis and paratestis
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