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An Update on Intracerebral Hemorrhage

An Update on Intracerebral Hemorrhage - A Cohort Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04783922
Enrollment
1000
Registered
2021-03-05
Start date
2021-03-17
Completion date
2022-02-28
Last updated
2021-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematoma, Intracerebral Hemorrhage, Stroke

Brief summary

The intracerebral hemorrhage study is a multicenter , combination of prospective and retrospective observational cohort study led by Dr. Muhammad Junaid Akram, PhD scholar at Chongqing Medical University. Prof Dr. Qi Li will be the senior consultant for the study. The study will be focusing on natural history, epidemiological , radiological, rehabilitative and clinical aspects as well as the effect of various treatments on the hemorrhagic patients. The study related data of the patients diagnosed with intracerebral hemorrhage will be collected in prospective and retrospective ways. The prognostic data for the patients will be assembled and collected via using different outcome measures at different points of time.

Detailed description

The study will be used to address the several key issues related to intracerebral hemorrhage. The demographics, scores based upon disease severity , mRS, GCS, NIHSS scores will be recorded at baseline and in the prospective and retrospective ways. The data obtained from the registered patients will be used for future use , critical review by expert neurologists, neurorehabilitative experts for further use and review.

Interventions

None listed

Sponsors

Shifa International Hospital
CollaboratorOTHER
Chongqing Medical University
CollaboratorOTHER
Shifa Clinical Research Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years Patients willing to participate via signing a consent form' Patients diagnosed with CT-Confirmed spontaneous intracerebral hemorrhage (ICH) Patients willing to participate in the follow up assessment

Exclusion criteria

* Not willing to participate Secondary ICH to hemorrhagic infarction or tumor bleeding etc. Traumatic ICH

Design outcomes

Primary

MeasureTime frameDescription
hematoma volume growth at 24 hours24 hoursTo assess early hematoma volume growth at 24 hours

Secondary

MeasureTime frameDescription
Early neurological deterioration assessed by NIHSS score at 24 hours24 hoursTo assess early neurological deterioration by using NIHSS score at 24 hours
Early neurological deterioration assessed by NIHSS score at 48 hours48 hoursTo assess early neurological deterioration by using NIHSS score at 48 hours
Early neurological deterioration assessed by NIHSS score at 72 hours72 hoursTo assess early neurological deterioration by using NIHSS score at 72 hours
Perihematomal edema volume measurement at 24 hours24 hoursTo measure the perihematomal edema volume growth at 24 hours
Functional outcome at 3 months assessed by modified Rankin Scale3 monthsAssess functional outcome at 3 months by using mRS
Perihematomal edema volume measurement at 72 hours72 hoursTo measure the perihematomal edema volume growth at 72 hours
Intraventricular hemorrhage growth24 hoursTo assess the presence of IVH at 24 hours
Major thrombotic events2 weeksTo assess the thrombotic events 2 weeks after admission
Perihematomal edema volume measurement at 48 hours48 hoursTo measure the perihematomal edema volume growth at 48 hours

Countries

Pakistan

Contacts

Primary ContactMuhammad Junaid Akram, DPT, MS-NMPT
drjunaidmalik2@gmail.com0092-335-1402214
Backup ContactMuhammad Junaid Akram
drjunaidmalik2@gmail.com0092-335-1402214

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026