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The efficacy of Palvix and Clopidex in Post-Stroke patients

Comparison between the efficacy of Plavix and Clopidex in Post stroke patients with Ischemic heart disease

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT201011025073N1
Enrollment
120
Registered
2012-12-23
Start date
2012-08-01
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

ischemic cerebrovascular stroke. Cerebral infarction due to embolism of cerebral arteries

Interventions

Intervention 1: Tablet Iranian Clopidegrol made by Exir Co. 75 mg daily for 1 month as the case group, one per day. Intervention 2: Tablet Plavix (75 mg) per os (orally) daily were used for control gr
Treatment - Drugs
Tablet Iranian Clopidegrol made by Exir Co. 75 mg daily for 1 month as the case group, one per day
Tablet Plavix (75 mg) per os (orally) daily were used for control group for one month, one per day

Sponsors

Baqiyatallah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: [Inclusion criteria]: Patients with Ischemic Heart Disease or ischemia; Patients consent for taking part in study; Patient cooperation in experiment pursuit and taking drugs; Patients shouldn’t be participating in any other clinical trial; Not having any drug taking record in the last month, [Exclusion criteria]: Existence of any hemorrhagic diseases, for instance peptic ulcer and inner-cranial hemorrhage; Existence of accompanied diseases interfering with drugs taken; Any record of allergy to Palvix or Clopidex; Any contraindications for taking Palvix or Clopidex. (Thrombocytopenia, liver disorders, Neutropenia-…); Those of patients who needed some mechanical hemodynamic support like using balloon pump; age more than 85 years and under 18 years.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Coagulation profile. Timepoint: baseline and one month later. Method of measurement: using platelet count, bleeding time and coagulation time.

Secondary

MeasureTime frame
Platelet aggrigation. Timepoint: baseline and one month later. Method of measurement: aggrigometery test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Majid Shohrati

Baqiayatallah University of Medical Sciences, Chemial Injuries Research Center

shohratimajid@yahoo.com+98 21 8860 0067

Outcome results

None listed

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