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Qi-Zhi-Tong-Luo Capsule in the Treatment of Patients after Ischemic Stroke at the Recovery Stage: a pilot study

Qi-Zhi-Tong-Luo Capsule in the Treatment of Patients after Ischemic Stroke at the Recovery Stage: a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002555
Enrollment
Unknown
Registered
2012-03-05
Start date
2010-11-16
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Ischemic Stroke

Interventions

Qizhi Group:Standard medical treatment + Qi-Zhi-Tong-Luo Capsules 4 capsules/time after breakfast and supper + 4 placebo capsules after lunch, for 4 weeks
Naoxintong Group:Standard medical treatment + Naoxintong Capsules 4 capsules tid, for 4 weeks

Sponsors

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. 35 to 80 years of age; 2. Symptoms consistent with ischemic stroke in the recovery stage, and without disorders of consciousness; 3. Symptoms consistent with Syndrome of "Qi-deficiency as well as Channel Obstruction by Tan and Blood-Stasis"; 4. Cerebral infarction is 2 weeks to 5 months, and FM score<95 and AQ<93.8; 5. Volunteer subjects, sign the informed consent certificates.

Exclusion criteria

Exclusion criteria: 1. TIA; 2. with cerebral hemorrhage in 6 months; 3. women with gestation or lactation; 4. allergic to the drug or tend to allergy; 5. stroke due to cerebral tumor, cerebral trauma or hematonosis etc. ; 6. stroke due to cerebral embolism; 7. complicated with some serious diseases as liver dysfunction, kidney dysfunction, hematonosisendocrine system diseases(except diabetics); 8. complicated with dysfunction of the joint; 9. complicated with mental disorder; 10. complicated with severe syptoms due to previous cerebral infarction which would influence the evaluation on the effect of this trial; 11. patient who has participated other trials.

Design outcomes

Primary

MeasureTime frame
Simplified Fugl-Meyer Assessment after 4 weeks;aphasia quotient after 4 week;

Secondary

MeasureTime frame
Zheng-hou Scales of Stoke after 4 weeks;Assessment of quality of life (QOL) after stroke;incidence of recurrent strok;

Countries

China

Contacts

Public ContactWang Zhong
zhonw@vip.sina.com+86 13601315446

Outcome results

None listed

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