Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01098643 · ClinicalTrials.gov registry record · NA
Satisfaction With Placement of Implantable Venous Access Devices in Patients With Solid Tumors
A NA study, sponsored by Vanderbilt University.
- Terminated
- Registry status
- NA
- Development phase
- 88
- Enrollment target
NCT01098643: Clinical Trial NA study, sponsored by Vanderbilt University.
NCT01098643 is a NA study that was terminated before completion, run by Vanderbilt University. The registered enrollment target is 88 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01098643, a NA study, was terminated before completion, sponsored by Vanderbilt University.
- TERMINATED
- Registry status
- NA
- Development phase
- 88 participants
- Enrollment target
Study Summary
RATIONALE: Gathering information about patients with solid tumors who have implantable venous access devices may help doctors learn more about patient satisfaction. PURPOSE: This phase I trial is studying satisfaction with placement of implantable venous access devices in patients with solid tumors.
Interventions
- OTHER medical chart review
- OTHER questionnaire administration
- OTHER survey administration
- OTHER computer-assisted intervention
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 88 participants |
| Start Date | 2009-10 |
| Est. Completion | 2011-09 |
| Phase | NA |
Why NCT01098643 stopped before completion
NCT01098643 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 88 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).
The record links to 0 conditions, and to 4 interventions - of which medical chart review is the first listed.
NCT01098643 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01098643 about?
NCT01098643 is a clinical study titled "Satisfaction With Placement of Implantable Venous Access Devices in Patients With Solid Tumors". RATIONALE: Gathering information about patients with solid tumors who have implantable venous access devices may help doctors learn more about patient satisfaction. PURPOSE: This phase I trial is studying satisfaction with placement of implantable venous access devices in patients with solid tumors...
What is the current status of trial NCT01098643?
This trial is currently terminated. It is a NA study. The enrollment target is 88 participants. The study started on 2009-10. Estimated completion is 2011-09.
What interventions are being tested in trial NCT01098643?
The interventions under investigation include: medical chart review (OTHER), questionnaire administration (OTHER), survey administration (OTHER), computer-assisted intervention (OTHER).
Who is sponsoring clinical trial NCT01098643?
This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01098643's enrollment target sits among peer trials
88 972nd of 2000 higher than 1,027 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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
- NCT03843463 · 88 participants · Phase 2
Escitalopram and Language Intervention for Subacute Aphasia
- NCT04066348 · 88 participants · Phase 2
TNF-α Treatment of Blast-Induced Tinnitus
- NCT04331704 · 88 participants · Phase 4
ANCHORS Alcohol & Sexual Health Study: UH3 Project
- NCT04536103 · 88 participants
Multi-Vendor Multi-Site Novel Accelerated MRI Relaxometry
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia