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Spots Global Cancer Trial Database for The Risk of Bleeding After Removal of Large Colorectal Polyps in Patients Taking Aspirin

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Trial Identification

Brief Title: The Risk of Bleeding After Removal of Large Colorectal Polyps in Patients Taking Aspirin

Official Title: The Risk of Bleeding After Removal of Large Colorectal Polyps in Patients Continuing or Discontinuing on Aspirin: a Multicenter, Double-blind, Placebo-controlled, Randomized Clinical Trial

Study ID: NCT01549418

Study Description

Brief Summary: The risk of bleeding after polypectomy of large colorectal polyps in patients taking aspirin is uncertain. This is a randomized, multi-center, placebo-controlled, double-blind study to compare the risk of significant bleeding after endoscopic polypectomy of large (\>=10mm) colorectal polyps in patients continuing or discontinuing on daily acetylsalicylic acid (ASA) use. Eligible patients will be randomly assigned in a 1:1 ratio to a group taking 75mg daily ASA or placebo 7 days before and 14 days following polypectomy. The primary endpoint of the study is bleeding within 30 days from colorectal polypectomy. The secondary endpoints are composite cardiovascular events occurring between the date of randomization and 30 days after polypectomy.

Detailed Description: Patients chronically taking aspirin (in prophylaxis doses 75-325 mg), with a diagnosis of colorectal polyps ≥ 10 mm in diameter will be enrolled on a routine polypectomy under hospitalization. Meeting the inclusion criteria, after informed consent and a cardiologist consent the patient will receive aspirin/placebo, and The Patient Diary to fill (Visit 1). The patient will be admitted to the Study Center in 6-7 days taking on the aspirin/placebo and prepared for the study (Visit 2). Patient will be under the care of a physician after polypectomy by a minimum of 6 hours. 14 days after polypectomy will be the first control visit, during which the physician will take back patient diary and pack treatment (Visit 3). 30 days after polypectomy will be the second control visit by phone (Visit 4). Patients will be monitored by looking at the end points.

Eligibility

Minimum Age: 40 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Contact Details

Name: Regula Jaroslaw, MD PhD

Affiliation: The Medical Centre for Postgraduate Education, and Center of Oncology Institute, Warsaw, Poland

Role: STUDY_DIRECTOR

Name: Kaminski F Michal, MD

Affiliation: The Medical Centre for Postgraduate Education, and Center of Oncology Institute, Warsaw, Poland

Role: STUDY_CHAIR

Name: Pisera Malgorzata, MSc

Affiliation: The Medical Centre for Postgraduate Education, and Center of Oncology Institute, Warsaw, Poland

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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