What is ALS Phase 3 Study Ceftriaxone?
Category: Others
See also: Clinical Trial
NCT00349622 is a clinical trial with ceftriaxone in subjects with amyotrophic lateral sclerosis (ALS). Other study IDs include: U01NS049640-02, NINDS, U01NS049640-02, NINDS CRC.
| Purpose | Patients | Evaluations | Perceived Effectiveness |
|---|---|---|---|
| Amyotrophic lateral sclerosis | 13 | 24 | |
| Participate in clinical trial | 10 | 12 |
- Major
- Moderate
- Slight
- None
- Can't tell
Side effects
Side effects as an overall problem
| Severity | Evaluations | Percentage |
|---|---|---|
| Severe | 2 | |
| Moderate | 11 | |
| Mild | 6 | |
| None | 15 |
Commonly reported side effects and conditions associated with ALS Phase 3 Study Ceftriaxone
| Side effect | Patients | Percentage |
|---|---|---|
| Gallstones | 3 | |
| Acid reflux | 1 | |
| Candida (fungal) infection | 1 | |
| Diarrhea | 1 | |
| Fever | 1 | |
| Flank pain | 1 |
Duration
Stopped using ALS Phase 3 Study Ceftriaxone
| Duration | Patients | Percentage |
|---|---|---|
| Less than 1 month | 2 | |
| 6 months - 1 year | 2 | |
| 1 - 2 years | 6 | |
| 2 - 5 years | 1 |
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