Trials / Completed
CompletedNCT06194578
A Study of Sterile Saline Infusion in Healthy Volunteers
A Phase 0, Single-Center Study to Evaluate the Safety and Tolerability of Injecting Sterile Saline Subcutaneously Into the Abdomen and Thigh of Healthy Volunteers Using Varying Volumes and Rates of Infusion
- Status
- Completed
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Janssen Research & Development, LLC · Industry
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Accepted
Summary
The purpose of the study is to evaluate the influence of needle size, injected fluid volume, and rate of fluid on the degree of pain experienced by adult healthy volunteers after subcutaneous infusion of sterile saline.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Sterile Saline | Sterile saline will be administered subcutaneously. |
Timeline
- Start date
- 2024-01-12
- Primary completion
- 2024-04-23
- Completion
- 2024-04-23
- First posted
- 2024-01-08
- Last updated
- 2025-05-23
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06194578. Inclusion in this directory is not an endorsement.