Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT05522153 · ClinicalTrials.gov registry record · Phase 1
Arista Hemostatic Powder for Total Knee Post Operative Outcomes Study
A Phase 1 study, sponsored by Virtua Health.
- Completed
- Registry status
- Phase 1
- Development phase
- 61
- Enrollment target
NCT05522153: Completed Phase 1 study, sponsored by Virtua Health.
NCT05522153 is a Phase 1 study that has completed, run by Virtua Health. The registered enrollment target is 61 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05522153, a Phase 1 study, has completed, sponsored by Virtua Health.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 61 participants
- Enrollment target
Study Summary
To examine in Arista hemostatic powder results in less post-total knee arthroplasty blood loss, hematoma formation, and improved range of motion when compared to patients who did not receive the product.
Primary Outcome
Calculated on standard hospital protocol
Interventions
- DRUG Arista
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 61 participants |
| Start Date | 2021-05-01 |
| Est. Completion | 2023-06-08 |
| Phase | Phase 1 |
What the finished NCT05522153 record still lists
NCT05522153 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 61 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 1 intervention - of which Arista is the first listed.
NCT05522153 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05522153 about?
NCT05522153 is a clinical study titled "Arista Hemostatic Powder for Total Knee Post Operative Outcomes Study". To examine in Arista hemostatic powder results in less post-total knee arthroplasty blood loss, hematoma formation, and improved range of motion when compared to patients who did not receive the product.
What is the current status of trial NCT05522153?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 61 participants. The study started on 2021-05-01. Estimated completion is 2023-06-08.
What interventions are being tested in trial NCT05522153?
The interventions under investigation include: Arista (DRUG).
Who is sponsoring clinical trial NCT05522153?
This trial is sponsored by Virtua Health, which has 9 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05522153's enrollment target sits among peer trials
61 828th of 2000 higher than 1,170 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT04115306 · 61 participants · Phase 1
Phase 1/1b/2 Study of Oral PMD-026 in Patients With Metastatic Breast Cancer
- NCT05070845 · 61 participants · Phase 2
Safety and Efficacy Study of PF-06835375 in Primary Immune Thrombocytopenia
- NCT05187832 · 61 participants · Phase 1
A Study of AND019 in Women With ER Positive HER2 Negative Advanced or Metastatic Breast Cancer
- NCT05269316 · 61 participants · Phase 1
Study to Evaluate IMP9064 as a Monotherapy or in Combination in Patients With Advanced Solid Tumors
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI