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Shuanling (Pentoxifylline sustained-release tablet) in the treatment for symptom improvement of dizziness/vertigo in acute ischemic stroke: Multicenter, control, open case registries

Shuanling (Pentoxifylline sustained-release tablet) in the treatment for symptom improvement of dizziness/vertigo in acute ischemic stroke: Multicenter, control, open case registries

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048426
Enrollment
Unknown
Registered
2021-07-06
Start date
2020-08-01
Completion date
Unknown
Last updated
2022-03-14

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

Conditions

Acute ischemic stroke

Interventions

observation group:pentoxifylline sustained-release tablets
control group:the guidelines for acute ischemic stroke recommend medication

Sponsors

Seventh Medical Center of PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Aged from 40 to 85 years; (2) Conformed to the diagnosis of acute ischemic stroke, confirmed by cranial CT or MRI examination, accompanied by dizziness /Vertigo, onset of 24h to within 7 days; (3) NIHSS score <=5 points.

Exclusion criteria

Exclusion criteria: (1) Exclude other peripheral vertigo such as benign paroxygenic positional vertigo; (2) Intracerebral hemorrhage, subarachnoid hemorrhage, hemorrhagic cerebral infarction, intracranial abnormal vascular network disease, brain tumor, tumor Stroke; (3) Patients with heart, liver, kidney, hematopoietic system and other serious primary diseases, in which ALT>=2.5 ULN; AST>=2.5 ULN, Cre >=1.5 ULN; (4) Pregnant or lactating women; (5) People with known allergic history to hexantheobromine, methylxanthine and basic therapeutic drugs; (6) Hypotension syndrome, systolic blood pressure <=110mmHg and diastolic blood pressure <=60mmHg; (7) Joint deformity affecting functional recovery; (8) gastrointestinal bleeding or ulcers, or nasal feeding can not take oral drugs and patients with definite bleeding tendency, long-term use anticoagulants (e.g., warfarin); (9) Other life-threatening or serious diseases with an expected survival period of less than 12 months; (10) Other disorders or psychiatric conditions that the investigator believes may limit neurological evaluation or patient follow-up; (11) Patients enrolled in other clinical trials within 30 days; (12) Other similar vasodilators were combined.

Design outcomes

Primary

MeasureTime frame
DARS;

Secondary

MeasureTime frame
VAS;mRS;

Countries

China

Contacts

Public ContactZhang Weiwei

The Seventh Medical Center of PLA General Hospital

zhangvivian@vip.sina.com+86 139 1077 4108

Outcome results

None listed

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