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Application of Noscapine in the treatment of stroke

The effect of Noscapine on first month mortality rate of massive ischemic strokes

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138809282886N1
Enrollment
60
Registered
2010-02-02
Start date
2008-04-05
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Massive Ischemic stroke. Stroke

Interventions

Intervention 1: Intervention: Noscapine syrup, three doses of 50 mg/day for 5 days. Intervention 2: Control: routine care.
Treatment - Drugs
Intervention: Noscapine syrup, three doses of 50 mg/day for 5 days

Sponsors

Iran university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: baseline National Institutes of Health Stroke Scale (NIHSS) level of consciousness >2 (no comatosis), motor function of arm and leg, totally >2, and total NIHSS score (excluding distal motor function) >7. Exclusion criteria: Modified Rankin Scale >2 prior to the onset of present stroke, patients whose neurological findings rapidly improve, patients with sepsis, meningitis or subarachnoid hemorrhage, post-seizure patients with a neurological deficit that could not be distinguished from Todd’s phenomenon, known presence or clinical suspicion of an intracranial neoplasm or mass lesion or sequelae to head trauma ,serious medical illnesses or conditions involving organ failure, such as severe congestive heart failure or severely compromised pulmonary, renal or hepatic function, respiratory dependence or unstable vital signs, a preexisting or concomitant medical, neurological or psychiatric disorder that could confound determination of the patient’s level of function or otherwise compromise the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Mortality. Timepoint: 1 month. Method of measurement: patient' s medical documents.

Secondary

MeasureTime frame
Drug's side effects. Timepoint: daily. Method of measurement: Reports of nurses and physicians.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mohamad Rezvani

Iran university of medical sciences

mrezvani55@gmail.com+98 21 6651 6001

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026