Stroke Clinical Trials

Find Stroke Clinical Trials Near You

Reduction of SystemiC Inflammation After Ischemic Stroke by Intravenous DNase Administration (ReSCInD)

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The goal of this (multicentric, randomised, placebo-controlled single-blinded; phase 2) clinical trial is to test the hypothesis that DNase 1 administration leads to a reduction in systemic immune response measured in patients after acute ischaemic stroke compared to control treatment. Participants will receive intravenous DNase 1 (500 µg/kg) or placebo (NaCl 0.9%) twice within 24±6 hours after symptom onset (last seen well). Blood samples will be taken at baseline, day 1 and 3. Personal visits will occur on baseline, day 1, 3 and discharge date. A telephone interview will be conducted on day 30±3.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with suspected acute ischemic stroke with symptom onset (last-seen-well) until Investigational drug application of less than 12 hours.

• Consent to participate in the study.

• Age ≥ 18 years.

• NIHSS ≥10 at admission.

Locations
Other Locations
Germany
Charité Universitätsmedizin
RECRUITING
Berlin
University Medical Center Hamburg-Eppendorf
RECRUITING
Hamburg
MHH Hannover
RECRUITING
Hanover
Institute for Stroke and Dementia Research, Ludwig Maximilian University Munich, University Hospital
NOT_YET_RECRUITING
Munich
TUM Klinikum München
NOT_YET_RECRUITING
Munich
Contact Information
Primary
Arthur Liesz, Prof. Dr.
arthur.liesz@med.uni-muenchen.de
+49 89 4400 46169
Time Frame
Start Date: 2026-10-01
Estimated Completion Date: 2028-07
Participants
Target number of participants: 36
Treatments
Active_comparator: Pulmozyme
Dornase alfa; intravenous administration; 500 µg/kg
Placebo_comparator: Isotonic Saline Solution
NaCl 0,9 %; intravenous administration; 0,5 ml/kg
Related Therapeutic Areas
Sponsors
Leads: Ludwig-Maximilians - University of Munich
Collaborators: University Hospital Erlangen, Universitätsklinikum Hamburg-Eppendorf

This content was sourced from clinicaltrials.gov