Hemorrhage Following Small Polyp Resection in the Colon in Anticoagulated Patients
NCT ID: NCT02375646
Last Updated: 2015-03-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
286 participants
INTERVENTIONAL
2015-05-31
2017-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This is a multicenter single-blinded prospective randomized trial comparing small post-polypectomy (polyps\<10mm) bleeding rates between two groups of patients: Continuous therapy with Warfarin, vs. LMW Heparin therapy while withholding Warfarin therapy (current practice).
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Prevention of Post-Polypectomy Colorectal Bleeding by Clips in Patients on Anticoagulants
NCT07007598
Safety of Continuing Anti-platelet Agents During Colonoscopic Polypectomy: A Prospective Study
NCT01647568
Tranexamic Acid During Colonic Endoscopic Resection Procedures
NCT05345613
Safety of Cold Snare Polypectomy in Patients With Uninterrupted Antiplatelet Agent
NCT04328987
The Effect of Tranexamic Acid on Intraoperative and Post-Operative Bleeding in Functional Endoscopic Sinus Surgery
NCT00671281
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Polyps up to 1 cm in diameter have been safely removed in patients on warfarin therapy. In one retrospective series, warfarin was discontinued 36 hours prior to colonoscopy to avoid supra therapeutic INR. 3 out of 123 patients who underwent 225 polypectomies on warfarin had bleeding, only one of which required treatment. All patients were prophylactically treated with clips.19 In a recent randomized trial, 70 patients with a total of 159 polyps up to 1 cm in diameter underwent polypectomy while taking warfarin. Patients were assigned to have their polyps removed either eith a cold snare technique or electrocautery. Immediate bleeding occurred in 10 of 70 patients (14%) and was more common in patients who had their polyps removed using electrocautery (23% vs 6%). No delayed bleeding occurred in the cold group whereas 5 (14%) patients required endoscopic hemostasis in the electrocautery group.
As immediate bleeding can be effectively managed endoscopically, the investigators should question if there is any potential benefit of periprocedural bridging in terms of preventing delayed bleeding (occurring during warfarin-LMWH overlap or following warfarin re-loading).
Considering the fact that \~ 25% of patients will be found to have colorectal polyps in screening colonoscopy, and that the majority of these polyps are \< 20 mm, A cardinal question is whether the investigators should keep choosing among the two traditional policies: advise all our patients to stop warfarin ahead of screening colonoscopies,Or keep them anticoagulated and reschedule them to a therapeutic colonoscopy in the face of discovering colonic polyps (an approach that was found to be cost effective in one study comparing these two policies).
The investigators think a third option might be better : keeping patients anticoagulated with warfarin, and perform polypectomies for polyps up to 20 mm, while re-scheduling patients with larger polyps.
To summarize, the three most important conclusions from the data presented in this introduction are:
1. Small polyps was shown to be safely removed under Warfarin
2. Delayed bleeding occurs after bridging is finished
3. Bridging therapy is probably related to increased bleeding, theoretically related to increased thromboembolic risk and is logistically complex Taken together, these background data underlies our logic to perform a prospective study comparing bleeding rates following polypectomies of small polyps in orally anticoagulated vs. bridged patients.
Hypothesis:In patients with moderate to high risk of thromboembolic events undergoing elective colonoscopy, a strategy of uninterrupted oral anticoagulation will lead to equivalent bleeding rates compared with conventional bridging anticoagulation.
Study Objectives:Primary study Objective : to evaluate the safety of polypectomy under Warfarin therapy compared to currently recommended bridging therapy with heparin or LMWH Study Design:Following signing on informed consent, patients on chronic Warfarin therapy meeting inclusion and exclusion criteria , who are scheduled for elective diagnostic colonoscopy will be randomly assigned to one of two groups, the first of which continue Warfarin treatment as usual while the second is switched to bridging therapy with LMWH according to recommendations of the ACCP guidelines. INR will be checked on the day before the colonoscopy (day -1) in both groups. Most recent CBC value (from recent 3 months) will serve as baseline value. If not available - CBC will be done during the recruitment period. On the day of colonoscopy (day 0), patients with INR values within therapeutic range or supratherapeutic value up to 0.5 units will proceed through colonoscopy. In case no INR value from day -1 is available, patient ambulatory INR values from the last three months will be reviewed and patient enrolled if \>=80% of values were within therapeutic window. The warfarin dose on day 0 will be taken only following the supervision period after the colonoscopy. In case the INR was more than 0.5 above therapeutic range on day -1, therapy will be resumed on day1. As to the colonoscopy, both groups will be scheduled to early morning and will be monitored for clinical follow up for 6 hours at Endoscopy unit. Polyps up to 10 mm (estimated using the open-forceps technique, forceps span=8mm) will be removed with cold or hot methods (according to physician preferences). Hemostatic clips will be applied if deemed necessary according to the performing physician judgement . In case of multiple polyps, the number of polypectomies done will be determined by the endoscopist. For polyps measuring \> 10 mm, colonoscopy will be rescheduled (but small polyps will still be removed during the index colonoscopy).Following the procedure, patients will be monitored for 6 hours at the Endoscopy unit. Delayed bleeding will be monitored by the patient on a daily follow up sheet. Ambulatory CBC will be done a week following the colonoscopy . Investigators will make Phone calls for follow up at day 5,10,14,30 . Outpatient clinic follow up will take place on day 30 ± 7 days.Patients will be instructed to contact the investigating physician in case of black stools or BRBPR or otherwise come to ER in case of any continuous bleeding or bleeding perceived to be significant by patient or family.
Study Procedures:Recruitment visit at GI institute outpatient clinics performed at least 1 week ahead of the Colonoscopy;Patient's primary care physician will be contacted by the study coordinator upon signing the informed consent, in order to perform necessary blood test before and after the procedure.; colonoscopy (day 0);Follow up period of 14 days via phone calls and patient sheets;Clinical follow up visit at day 30 Sample Size:The bleeding rate post polypectomy in orally anticoagulated patient undergoing polypectomy of small polyps on Warfarin was reported to be as low as 1% in recent trials (see background). The rate of postpolypectomy bleeding in the general population is 1-2.5% . As bridging was found to increase bleeding compared to no bridging in the largest available meta-analysis, the investigators assume a bleeding rate of 4% in the bridging group. The sample size was estimated based on the complicated rates of delayed bleeding within 2 weeks after polypectomy and was based on detecting equivalence in proportions at the 5% level of significance with a power of 80%, yielding a sample size of 286 (143 each group) .
Statistical Analysis:Descriptive statistics including 95% CIs will be calculated for all baseline variables using means, medians, SDs and interquartile ranges for continuous variables and rates and proportions for discrete variables for each treatment arm. For the primary outcome, clinically significant bleeding, treatment arms will be compared using chi-square test. Baseline characteristics will be compared and, if any clinically significant differences are identified, a logistic regression analysis will be conducted to compare clinically significant bleeding in between the two treatment arms adjusting for these differences. Same analysis will be followed for the secondary outcomes.
Ethical issues:The investigator will ensure that this study is conducted in accordance with the principles of the "Declaration of Helsinki" guidelines and with the laws and regulations of the state of Israel.
Written informed consent must be obtained prior to participation in the study.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Continued Warfarin
continuous Warfarin therapy (aiming for therapeutic INR: 2-3) will be given throughout the study
Warfarin
LMW Heparin
Enoxaparin 1mg/kg SC bid (adjusted to renal function) will be given 5 days before the colonoscopy while withholding therapy with Warfarin. The day after procedure Warfarin therapy will be added, and Enoxaparin stopped when therapeutic INR will be reached
LMW Heparin
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Warfarin
LMW Heparin
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patient aged 40-75 undergoing colonoscopy
* On warfarin therapy
Exclusion Criteria
* Known Polyps \> 10 mm
* Baseline Anemia \< 10 gr%
* NOACs based anticoagulation
* Concomitant Mandatory Aspirin therapy (in 6 months period following ACS)
* Dual antiplatelet therapy
* Known bleeding diathesis
* Severe hepatic or renal impairment
* Previous history of procedure related major bleeding
* History of noncompliance to medical therapy
* Prior HIT
* Included in another clinical trial
* Inability to comply with written daily reporting on dedicated
40 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Rambam Health Care Campus
OTHER
Carmel Medical Center
OTHER
Soroka University Medical Center
OTHER
Tel Aviv Medical Center
OTHER
Hadassah Medical Organization
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Eran Israeli
Head, IBD Unit, Institute of Gastroenterology and Liver Diseases
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
References
Explore related publications, articles, or registry entries linked to this study.
ASGE Standards of Practice Committee; Anderson MA, Ben-Menachem T, Gan SI, Appalaneni V, Banerjee S, Cash BD, Fisher L, Harrison ME, Fanelli RD, Fukami N, Ikenberry SO, Jain R, Khan K, Krinsky ML, Lichtenstein DR, Maple JT, Shen B, Strohmeyer L, Baron T, Dominitz JA. Management of antithrombotic agents for endoscopic procedures. Gastrointest Endosc. 2009 Dec;70(6):1060-70. doi: 10.1016/j.gie.2009.09.040. Epub 2009 Nov 3. No abstract available.
Birnie DH, Healey JS, Wells GA, Verma A, Tang AS, Krahn AD, Simpson CS, Ayala-Paredes F, Coutu B, Leiria TL, Essebag V; BRUISE CONTROL Investigators. Pacemaker or defibrillator surgery without interruption of anticoagulation. N Engl J Med. 2013 May 30;368(22):2084-93. doi: 10.1056/NEJMoa1302946. Epub 2013 May 9.
Horiuchi A, Nakayama Y, Kajiyama M, Tanaka N, Sano K, Graham DY. Removal of small colorectal polyps in anticoagulated patients: a prospective randomized comparison of cold snare and conventional polypectomy. Gastrointest Endosc. 2014 Mar;79(3):417-23. doi: 10.1016/j.gie.2013.08.040. Epub 2013 Oct 11.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
0446-14-HMO
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.