- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04502498
Preoperative Subclinical DVT Screening in Locally Advanced Bladder Cancer Patients Candidate for Radical Cystectomy.
August 6, 2020 updated by: Samer Morsy, Kasr El Aini Hospital
Preoperative Detection of Subclinical Lower Limb Deep Venous Thrombosis in Locally Advanced Bladder Cancer Patients Candidate for Radical Cystectomy
Preoperative subclinical DVT screening in locally advanced bladder cancer patients candidate for radical cystectomy.
Study Overview
Status
Unknown
Intervention / Treatment
Detailed Description
60 patient with local advanced bladder cancer are subjected to preoperative lower limb duplex within 1 week preoperative to radical cystectomy
Study Type
Observational
Enrollment (Anticipated)
60
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Locally advanced Bladder cancer patients candidate for radical cystectomy and with no symptoms of DVT
Description
Inclusion Criteria:
- any age
- Any sex
- Muscle invasive bladder cancer local advanced patients candidate for radical cystectomy
Exclusion Criteria:
- Unfit patients
- any contraindication for surgery
- obese
- coagulopathy
- bedridden
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
60 patients with local advanced bladder cancer
Local advanced bladder cancer patients candidate for radical cystectomy
|
Lower limb duplex and doppler one week before radical cystectomy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Preoperative subclinical DVT
Time Frame: 6 months
|
Asymptomatic patients candidate for radical cystectomy
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ANTICIPATED)
October 1, 2020
Primary Completion (ANTICIPATED)
June 1, 2021
Study Completion (ANTICIPATED)
October 1, 2021
Study Registration Dates
First Submitted
August 4, 2020
First Submitted That Met QC Criteria
August 4, 2020
First Posted (ACTUAL)
August 6, 2020
Study Record Updates
Last Update Posted (ACTUAL)
August 10, 2020
Last Update Submitted That Met QC Criteria
August 6, 2020
Last Verified
August 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Cairo University Hospital
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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