Hyponatremia Clinical Trial
Official title:
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)
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 |
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.
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 |
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator)
Country | Name | City | State |
---|---|---|---|
United States | Thomas Jefferson University | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Thomas Jefferson University | Valeant Pharmaceuticals International, Inc. |
United States,
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 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06037928 -
Plasma Sodium and Sodium Administration in the ICU
|
||
Recruiting |
NCT04561531 -
Efficacy and Safety of Bolus Comparing With Continuous Drip of 3% NaCl in Patients With Severe Symptomatic Hyponatremia.
|
N/A | |
Terminated |
NCT02012959 -
Study of the Safety and Effectiveness of SAMSCA® (Tolvaptan) in Children and Adolescents With Euvolemic or Hypervolemic Hyponatremia
|
Phase 3 | |
Recruiting |
NCT02936167 -
Comparison of Ringer Lactate and Isotonic Acetate Solution as Perioperative Maintenance Fluid for Children
|
N/A | |
Completed |
NCT00621348 -
Maintenance Intravenous Fluids in Children
|
Phase 3 | |
Terminated |
NCT03703713 -
Colloid Osmotic Pressure and Osmolality in Hyponatremia
|
||
Completed |
NCT02926989 -
Intravenous Fluids in Hospitalised Children
|
Phase 4 | |
Terminated |
NCT02959411 -
Tolvaptan for Advanced or Refractory Heart Failure
|
Phase 4 | |
Completed |
NCT02573077 -
An Observational Study Measuring Outcomes in Cancer Patients Treated for Moderate to Severe Hyponatremia in Italy
|
||
Withdrawn |
NCT02667977 -
Reexamining Hypotonic Intravenous Fluid Use
|
N/A | |
Terminated |
NCT01708811 -
Hyponatremia and Myometrium Contractility. An Invitro Study
|
N/A | |
Withdrawn |
NCT01326429 -
Frequency and Origin of Dysnatremias in the Emergency Department
|
N/A | |
Completed |
NCT01456533 -
Copeptin in the Differential Diagnosis of Dysnatremia in Hospitalized Patients
|
N/A | |
Terminated |
NCT01227512 -
Effects of Tolvaptan vs Fluid Restriction in Hospitalized Subjects With Dilutional Hyponatremia
|
Phase 3 | |
Recruiting |
NCT06013800 -
Hyponatremia Volume Status Analysis by Point-of-care Ultrasound
|
||
Terminated |
NCT04020926 -
Impact of Hyponatremia on Muscle Strength, Gait and Cognitive Function
|
||
Withdrawn |
NCT02442674 -
A Trial of Tolvaptan in Children and Adolescent Subjects With Euvolemic and Hypervolemic Hyponatremia
|
Phase 3 | |
Completed |
NCT02545101 -
An Observational Study on Real-world Use and Outcomes of Patients Treated With Tolvaptan for Hyponatraemia Due to SIADH
|
N/A | |
Terminated |
NCT02215148 -
Pharmacokinetics and Clinical Response of Tolvaptan in Neurocritical Care Patients
|
N/A | |
Recruiting |
NCT01748331 -
The Effect of Fluid Restriction in Congestive Heart Failure Complicated With Hyponatremia
|
N/A |