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NCT05625373 · ClinicalTrials.gov registry record · Phase 2
The Effect of Intrawound Vancomycin Powder on Surgical Site Infection in Inguinal Lymph Node Dissection
A Phase 2 study of Postoperative Complications, sponsored by Women and Infants Hospital of Rhode Island.
- Recruiting
- Registry status
- Phase 2
- Development phase
- 30
- Enrollment target
- 1
- Study location
NCT05625373 is a Phase 2 study of Postoperative Complications that is actively recruiting participants, run by Women and Infants Hospital of Rhode Island. The registered enrollment target is 30 participants, below the 385-participant average among 17 other Postoperative Complications trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05625373, a Phase 2 study of Postoperative Complications, is actively recruiting participants, sponsored by Women and Infants Hospital of Rhode Island.
- RECRUITING
- Registry status
- Phase 2
- Development phase
- 30 participants
- Enrollment target
- 1
- Study location
Study Summary
The study will be a pilot randomized control trial with a 1:1 patient randomization of vancomycin powder placement at the time of surgery (compared to no vancomycin placement) with the goal of reducing postoperative complications in patients undergoing an inguinal lymph node dissection for vulvar cancer. The primary objective is to measure the composite rate of postoperative complications within 30 days of inguinal lymph node dissection in patients with vulvar cancer.
Conditions Studied
Interventions
- DRUG Vancomycin
Study Locations (1)
Rhode Island
- Women and Infants Hospital - Providence
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2022-10-25 |
| Est. Completion | 2024-08-30 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05625373
The ClinicalTrials.gov registry entry for NCT05625373 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 385-participant average among 17 other Postoperative Complications trials with a reported enrollment target (92% lower). The listed sponsor is Women and Infants Hospital of Rhode Island, which has 65 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Postoperative Complications appearing as the primary indexed condition, and to 1 intervention - of which Vancomycin is the first listed.
NCT05625373 reports 1 study location spanning 1 distinct geographic area - top geographies include Rhode Island.
Frequently Asked Questions
What is clinical trial NCT05625373 about?
NCT05625373 is a clinical study titled "The Effect of Intrawound Vancomycin Powder on Surgical Site Infection in Inguinal Lymph Node Dissection". The study will be a pilot randomized control trial with a 1:1 patient randomization of vancomycin powder placement at the time of surgery (compared to no vancomycin placement) with the goal of reducing postoperative complications in patients undergoing an inguinal lymph node dissection for vulvar ca...
What is the current status of trial NCT05625373?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2022-10-25. Estimated completion is 2024-08-30.
What conditions does trial NCT05625373 study?
This clinical trial studies the following conditions: Postoperative Complications.
What interventions are being tested in trial NCT05625373?
The interventions under investigation include: Vancomycin (DRUG).
Who is sponsoring clinical trial NCT05625373?
This trial is sponsored by Women and Infants Hospital of Rhode Island, which has 65 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05625373 being conducted?
This trial has 1 study location across Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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