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WithdrawnNCT02074254Updated Nov 10, 2021

Safety of Percutaneous Tracheostomy in Clopidogrel and Selective Serotonin Reuptake Inhibitors

An observational study in Tracheostomy Complication, sponsored by Ohio State University. Withdrawn at 2 sites in United States. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2021-11-10.

Sponsored by Ohio State University · Observational

Why this study was withdrawn
Not sure. PI is no longer at OSU.
Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
0
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Safety of Percutaneous Tracheostomy in Clopidogrel and Selective Serotonin Reuptake Inhibitors

Read the detailed description

We propose a retrospective review of our experience with bleeding complication in the presence of antiplatelet and SSRI therapy and compare the complications with those who were not on antiplatelet agents or SSRI.

02

Conditions studied

  • Tracheostomy Complication
03

In context

Lead sponsor

Ohio State University is the lead sponsor of 640 studies on the registry; 144 are open to participants now.

Of its 60 completed or terminated interventional studies of FDA-regulated products, 45 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study is being done to evaluate the safety of percutaneous tracheostomy in patients taking antiplatelet agents such as aspirin and/ or clopidogrel or selective serotonin reuptake inhibitors. We will identify all patients age 18 or older who have undergone percutaneous tracheostomy by interventional pulmonology at OSUMC and access their PHI to record variables (see data collection form).

Inclusion criteria

  • on antiplatelet therapy or selective serotonin reuptake inhibitors(SSRI)

Exclusion criteria

Exclusion Criteria:

  • N/A
05

Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
0 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. a retrospective review of our experience with bleeding complication in the presence of antiplatelet and SSRI therapy and compare the complications with those who were not on antiplatelet agents or SSRI

    Time frame: 24 months

07

Study locations

2 sites
  • OSUMC
    Columbus, Ohio 43210, United States
  • University Hospital, OSUMC 473 W 12th Ave
    Columbus, Ohio 43210, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 10, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02074254
Lead sponsor
Ohio State University
Responsible party
Sponsor
First posted
Feb 28, 2014
Start date
Mar 22, 2012
Primary completion
May 9, 2012 (estimated)
Completion
May 9, 2012 (estimated)
Last update
Nov 10, 2021

Study contacts

Shaheen Islam, MD
principal investigator · Ohio State University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Nov 2021. You cannot join it, but the record below documents what was studied.

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