Trials / Unknown
UnknownNCT04887896
Assessing GS500 in Functional Constipation
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study Assessing the Effect of GS500 in Subjects With Functional Constipation
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 260 (estimated)
- Sponsor
- Gelesis, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This study is designed to evaluate the safety, tolerability and efficacy of GS500 as a superabsorbent hydrogel for relief of constipation in subjects with functional constipation.
Detailed description
To evaluate the safety, tolerabilityand efficacy of GS500 as a superabsorbent hydrogel for relief of constipation in subjects with functional constipation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | GS500 | Device: GS500 |
| DEVICE | Placebo | Device: Placebo |
Timeline
- Start date
- 2022-07-15
- Primary completion
- 2023-12-30
- Completion
- 2023-12-30
- First posted
- 2021-05-14
- Last updated
- 2022-01-24
Source: ClinicalTrials.gov record NCT04887896. Inclusion in this directory is not an endorsement.