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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01299779
Other study ID # #10C.29
Secondary ID
Status Completed
Phase N/A
First received July 12, 2010
Last updated June 4, 2013
Start date June 2010
Est. completion date September 2012

Study information

Verified date June 2013
Source Thomas Jefferson University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Objective: To compare the incidence of peri-colonoscopy hyponatremia associated with PEG 3350 + sports drink (PEG-SD) versus PEG 3350-electrolyte solution + sodium sulfate + sodium ascorbate and ascorbic acid (PEG-ELS).

Hypothesis: As compared to PEG-SD, hyponatremia occurs significantly less often with PEG-ELS.


Description:

Looking at the Incidence of Hyponatremia With Two Commonly Prescribed Purgatives for Colonoscopy-Polyethylene Glycol 3350 With a Sports Drink (PEG-SD) Compared to Polyethylene Glycol 3350 With Electrolyte Solution (PEG-ELS)


Recruitment information / eligibility

Status Completed
Enrollment 460
Est. completion date September 2012
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adults age 18 years or older scheduled for elective outpatient colonoscopy: 8am - noon.

Exclusion Criteria:

- Unable or unwilling to consent

- Pregnant

- Breast feeding

- Significant psychiatric illness

-> 50% colon resection

- Bowel obstruction

- History of hyponatremia (Serum sodium <135 mmol/L)

- End stage renal disease on dialysis

- History of chronic kidney disease (other than kidney stones)

- Decompensated cirrhosis, including:

- History of bleeding due to portal hypertension (varices, gastropathy, etc) within 3 months

- Hepatic encephalopathy (not controlled with medications) within 3 months

- Clinical presence of ascites

- Active cardiac disease

- Recent myocardial infarction (<4weeks)

- Unstable angina

- Congestive heart failure NYHA Functional Class Stage III or IV

- Stage III: Marked limitation of activity. Less than ordinary activity (e.g. walking short distances, 20-100 m) causes fatigue, palpitations, dyspnea. Comfortable at rest.

- Stage IV: Severe limitations. Experiences symptoms even while at rest. Mostly bedbound patients.

Exclusion Criteria (post-enrollment), from baseline labs:

- Serum creatinine > 1.5 mg/dL

- Serum potassium < 3.3 or > 5.5 mmol/L

- Serum sodium < 135 mmol/L or >150 mmol/L

- Serum calcium < 8.0 or > 11.0 mg/dL

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator)


Related Conditions & MeSH terms


Intervention

Drug:
PEG-SD
PEG-SD Bisacodyl: two 5-mg tablets at 3 pm day prior 1L sports drink* (labeled #1) with PEG-3350 119 gram bottle (labeled #1) at 6 pm night prior 1L SD* (labeled #2) with PEG-3350 119 gram bottle (labeled #2) starting 4 hrs prior to colonoscopy Same flavor, non-red Gatorade® for all patients.
PEG-ELS
1L + 500 cc clear liquids at 6 pm night prior 1L + 500 cc clear liquids starting 4 hours prior to colonoscopy

Locations

Country Name City State
United States Thomas Jefferson University Philadelphia Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Thomas Jefferson University Valeant Pharmaceuticals International, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Development of hyponatremia in the peri-colonoscopy period blood drawn 30 minutes post colonoscopy Yes
Secondary Development of serum electrolytes levels outside the normal range for Sodium, chloride, potassium, calcium blood drawn 30 minutes post colonoscopy Yes
Secondary Change from baseline for serum electrolytes Sodium, chloride, potassium, calcium blood drawn 30 minutes post colonoscopy Yes
Secondary Change in renal function from baseline Creatinine, calculated GFR blood drawn pre colonoscopy and 30 minutes post colonoscopy Yes
Secondary Changes in the following from baseline a. Serum vasopressin b. Serum osmolality c. Urine electrolytes and osmolality blood drawn pre colonoscopy and 30 minutes post colonoscopy Yes
Secondary Serum cortisol and TSH levels for only patients who develop hyponatremia blood drawn 30 minutes post colonoscopy Yes
Secondary Hemodynamic/volume changes at baseline and immediately prior to colonoscopy Weight
Blood pressure supine and upright - systolic, diastolic
Pulse supine and upright
Development of orthostatic change: yes/no
Development of orthostatic symptoms - light-headed, dizzy, diaphoretic, etc.: yes/no
hemodynamic measurments taken pre and post colonoscopy Yes
Secondary Adverse Events - Incidence and severity using 10-point Likert scale GI - nausea, vomiting, abdominal pain, bloating
Light headedness
1 hour post colonoscopy assessment Yes
Secondary Prep Completion: <90% vs. > 90% one time assessment pre colonoscopy No
Secondary Indication for colonoscopy: Screen/Surveillance vs. Symptom one time assessment pre colonoscopy No
Secondary Assessment of independent risk factors for hyponatremia Age
Sex
Race
Medications
Medical history
BMI
Anxiety - Beck scale
Fluid intake for 24 hours prior to colonoscopy (not including the prep or fluids required to accompany the prep); patients will be shown a liter container to assist with their estimate.
i. Less than 3 Liters ii. 3-5 liters iii. More than 5 liters
one time assessment pre colonoscopy No
Secondary Efficacy Whole colon prep: adequate (excellent/good) vs. inadequate (fair/poor)
Cecal or small bowel intubation - Yes/No
endoscopist will evaluate during colonoscopy No
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