Trials / Completed
CompletedNCT02808325
Study on the Efficacy and Safety of Gelaspan
Prospective Controlled Randomized Double-blind Multicentre Study in Parallel Groups on the Efficacy and Safety of Gelaspan in Combination With Sterofundin ISO in Comparison With Gelofusine in Combination With Sodium Chloride Braun in Patients Scheduled for Abdominal or Pelvic Surgery
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 72 (actual)
- Sponsor
- B. Braun Medical LLC · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
It is the objective of the study to investigate the efficacy and safety of two different volume replacement regimens with gelatine solutions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Gelaspan 4% | Gelaspan 4% combined with Sterofundin ISO |
| DRUG | Gelofusine 4% | Gelofusine 4% combined with Sodium Chloride |
Timeline
- Start date
- 2016-06-01
- Primary completion
- 2017-06-01
- Completion
- 2017-06-01
- First posted
- 2016-06-21
- Last updated
- 2017-08-11
Locations
3 sites across 1 country: Russia
Source: ClinicalTrials.gov record NCT02808325. Inclusion in this directory is not an endorsement.