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The effects of Propranolol combined with Metoclopramide on stroke-associated pneumonia and related immune indicators: a clinical randomized controlled trial

A Randomized Controlled Trial of Propranolol Combined with Metoclopramide for Stroke-Associated Pneumonia and Its Impact on Immune Parameters

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111972
Enrollment
Unknown
Registered
2025-11-07
Start date
2023-10-01
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Cerebrovascular structural and functional abnormalities and related diseases

Interventions

Propranolol combined with Metoclopramide treatment group:Propranolol 10 mg + metoclopramide 5 mg + normal saline 10ml nasal feeding, three times a day
standard acute cerebral infarction treatment program (including antiplatelet or anticoagulation, lipid regulation, etc.) or standard cerebral hemorrhage treatment program, standard nasogastric enteral
Propranolol group:Propranolol 10 mg + normal saline 10 ml was administered by nasogastric feeding three times a day
standard acute cerebral infarction treatment regimen (including antiplatelet or anticoagulation, lipid regulation, etc.) or standard cerebral hemorrhage treatment regimen, standard nasogastric enteral
Metoclopramide group:Metoclopramide 5 mg + normal saline 10ml nasal feeding, three times a day

Sponsors

Quanzhou First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosis meets the diagnostic criteria for acute cerebral infarction in the "Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2018" or the diagnostic criteria for cerebral hemorrhage in the "Chinese Guidelines for the Diagnosis and Treatment of Cerebral Hemorrhage 2019"; 2. Age > 18 years; 3. Onset time < 48 hours; 4. Swallowing difficulty determined by the Watanabe water swallowing test, requiring nasogastric feeding.

Exclusion criteria

Exclusion criteria: 1. Presence of contraindications to propranolol or metoclopramide; 2. Dysphagia prior to onset; 3. Existing infection at the time of admission; 4. Use of ß-blockers (including selective and non-selective ß-blockers), metoclopramide, or antibiotics within the past 7 days; 5. Patients with an expected survival of no more than 14 days.

Design outcomes

Primary

MeasureTime frame
the severity of stroke;

Secondary

MeasureTime frame
swallowing function;

Countries

China

Contacts

Public ContactPingzhen Lin

Quanzhou First Hospital

lpz385675123@163.com+86 188 5951 3930

Outcome results

None listed

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