CLINICAL TRIALS PROFILE FOR MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
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All Clinical Trials for magnesium sulfate; potassium sulfate; sodium sulfate
| Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
|---|---|---|---|---|---|---|
| NCT01928082 ↗ | The Effects of Estrogen Replacement Therapy in Postmenopausal Women With Hypercalciuria and Low Bone Mass | Terminated | University of Chicago | Phase 2 | 2013-08-01 | The purpose of this study is to assess if estrogen replacement normalizes urinary calcium excretion in postmenopausal women with hypercalciuria and low bone mass and to assess for differences in response to estrogen replacement in women with familial hypercalciuria compared to nonfamilial hypercalciuria. |
| NCT02124447 ↗ | Single Center Comparison of 4 FDA Approved, Commercially Available Bowel Purgatives for Colonoscopy | Withdrawn | Medical College of Wisconsin | N/A | 2014-06-01 | This will be a 4-way comparison to prospectively evaluate the efficacy and patient tolerability of four commercially available bowel preparations among patients undergoing colonoscopy for screening and surveillance in a single tertiary academic medical center. |
| NCT02523911 ↗ | Efficacy and Tolerability of Suprep With and Without Simethicone for Routine Colonoscopy for Colorectal Cancer Screening | Withdrawn | Mercy Medical Center, Des Moines, Iowa | N/A | 2016-03-01 | The purpose of this study is to investigate Suprep bowel preparation, with and without the anti-gas medication simethicone, in terms of efficacy and patient tolerability in the preparation of patients undergoing routine colonoscopy for colorectal cancer screening. |
| NCT02523911 ↗ | Efficacy and Tolerability of Suprep With and Without Simethicone for Routine Colonoscopy for Colorectal Cancer Screening | Withdrawn | MercyOne Des Moines Medical Center | N/A | 2016-03-01 | The purpose of this study is to investigate Suprep bowel preparation, with and without the anti-gas medication simethicone, in terms of efficacy and patient tolerability in the preparation of patients undergoing routine colonoscopy for colorectal cancer screening. |
| NCT03299452 ↗ | Clinical Studies by Using Alphacait to Screen Drugs for Advanced Solid Tumor | Unknown status | Alphacait, LLC | Phase 2 | 2017-01-01 | This is a single-center, open-label, single-arm, non-randomized study designed to evaluate PFS, safety, overall survival (OS), objective response rate (OPR), disease control rate (DCR) and biomarkers of cancer therapy based on Alphacait screening system in subjects with advanced malignant tumor. |
| NCT03299452 ↗ | Clinical Studies by Using Alphacait to Screen Drugs for Advanced Solid Tumor | Unknown status | Haining Health-Coming Biotech Co., Ltd. | Phase 2 | 2017-01-01 | This is a single-center, open-label, single-arm, non-randomized study designed to evaluate PFS, safety, overall survival (OS), objective response rate (OPR), disease control rate (DCR) and biomarkers of cancer therapy based on Alphacait screening system in subjects with advanced malignant tumor. |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
Clinical Trial Conditions for magnesium sulfate; potassium sulfate; sodium sulfate
Condition Name
| Condition Name for magnesium sulfate; potassium sulfate; sodium sulfate | |
| Intervention | Trials |
| Patients Undergoing Screening or Surveillance Colonoscopy | 1 |
| Bowel Preparation for Colonoscopy | 1 |
| Colon Disease | 1 |
| Colorectal Cancer | 1 |
| [disabled in preview] | 0 |
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Clinical Trial Locations for magnesium sulfate; potassium sulfate; sodium sulfate
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Clinical Trial Progress for magnesium sulfate; potassium sulfate; sodium sulfate
Clinical Trial Phase
Clinical Trial Sponsors for magnesium sulfate; potassium sulfate; sodium sulfate
Sponsor Name
