Safety and Efficacy of Remimazolam in ASA III and IV Patients Undergoing Colonoscopy



Status:Completed
Conditions:Gastrointestinal
Therapuetic Areas:Gastroenterology
Healthy:No
Age Range:18 - Any
Updated:1/25/2019
Start Date:November 2015
End Date:December 2016

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A Study Evaluating the Safety and Efficacy of Remimazolam (CNS 7056) Compared to Placebo and Midazolam in ASA III and IV Patients Undergoing Colonoscopy

A prospective, double-blind, randomized, placebo and active controlled, multi-center,
parallel group study comparing remimazolam to placebo, with an additional open-label arm for
midazolam, in American Society of Anesthesiologists (ASA) Grade III and IV patients (ASA
status evaluated by an anesthesiologist not otherwise involved in the study) undergoing a
colonoscopy for diagnostic or therapeutic reasons.


Inclusion Criteria:

1. Male and female patients, aged ≥18, scheduled to undergo a diagnostic or therapeutic
colonoscopy (therapeutic procedures may include hemostasis, resection, ablation
decompression, and foreign body extraction, for example).

2. ASA grade III/IV

1. ASA III patients are patients with severe systemic disease eg patients who, in
the judgment of the Principal Investigator (PI), have significant enough systemic
disease to warrant performing the colonoscopy procedure only in a facility which
has post-procedure inpatient capability. ASA III physical status classification
encompasses a wide range of potential patient co-morbidities some of which may
make the selection of a facility with post-procedure inpatient capability
preferable. By definition, ASA III patients have one or more moderate to severe
systemic diseases which potentially cause substantial functional limitation.
Examples may include poorly controlled diabetes or hypertension, moderate to
severe chronic obstructive pulmonary disease, active hepatitis, heart failure or
coronary artery disease (including implanted pacemaker and/or stent, recent
myocardial infarction) cerebrovascular accident, or end stage renal disease
requiring dialysis.

2. ASA IV patients are patients with severe systemic disease that is a constant
threat to life eg at least one severe disease that is poorly controlled or at end
stage; possible risk of death; unstable angina; symptomatic chronic obstructive
pulmonary disease; symptomatic chronic heart failure; hepatorenal failure.

3. For all female patients, negative result of urine or serum pregnancy test.
Additionally, for women with child-bearing potential only, use of birth control during
the study period (from the time of consent until all specified observations are
completed).

4. Patient voluntarily signs and dates an informed consent form (ICF) that is approved by
an investigational review board (IRB) prior to the conduct of any study procedure.

5. Patient is willing and able to comply with study requirements and will be available
for a Follow-up Visit on Day 1 (+ 1 day) and Follow-up Phone call (Day 4 +/- 3 days)
after the colonoscopy.

Exclusion Criteria:

1. Patients with a known sensitivity to benzodiazepines, flumazenil, opioids, naloxone,
or a medical condition such that these agents are contraindicated.

2. Female patients with a positive pregnancy test at screening or baseline and lactating
female patients.

3. Patients clearly acutely intoxicated with alcohol or drugs of abuse at baseline.

4. Patients in receipt of any investigational drug within 30 days or less than 7
half-lives (whichever is longer) before Screening, or scheduled to receive one during
the study period.

5. Participation in any previous clinical trial with remimazolam.

6. Patients with an inability to communicate well with the Investigator, or deemed
unsuitable according to the Investigator (in each case providing a reason).
We found this trial at
3
sites
Jupiter, Florida 33458
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Jupiter, FL
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Indianapolis, IN
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Monroe, Louisiana 71201
Phone: 318-807-0819
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Monroe, LA
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