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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02022527
Other study ID # PEU2013
Secondary ID
Status Recruiting
Phase Phase 4
First received December 20, 2013
Last updated December 26, 2013
Start date June 2013

Study information

Verified date December 2013
Source Pharmacoeconomic Unit, Egypt
Contact Gihan H Elsisi, Msc
Phone +201227366018
Email gihan-elsisi@hotmail.com
Is FDA regulated No
Health authority Egypt: Ministry of Health and Population
Study type Interventional

Clinical Trial Summary

The combined Antiplatelet and Anticoagulant treatment decreased thrombus formation and overall mortality. Also the initiation of an efficacious early anticoagulation protocol is important because of its potential impact on the rate of early thromboembolic complications after mechanical valve implantation. An important question that remains to be answered is whether the combination would be cost effective than Warfarin alone, with a reduction in major bleeding. In addition, the knowledge about its cost-effectiveness has not yet been established in Egypt. The aim of this trial based economic evaluation is to conduct a cost-effectiveness analysis for combination of low-dose Aspirin and Warfarin versus Warfarin alone in prosthetic valve patients from the medical provider perspective specially that a misconception is still existed between the physicians in Egypt that the cost of complications is not worthy so our main aim is to test the cost of complications.


Description:

The measurements will be assessed:

A- Number of patients improved during follow up:

1. Demographic data

2. Diagnosis

3. Laboratory tests (CBC, Prothrombin Time, liver and renal function tests)

4. Echocardiography profile

B-Costs:

Direct medical costs will be assessed directly from hospital's records and tender lists.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender Both
Age group 15 Years to 50 Years
Eligibility Inclusion Criteria:

Patients operated in Ain Shams University Hospitals for aortic and/ or mitral valve replacement.

Exclusion Criteria:

- Congenital blood disorders, Hemophilia.

- Advanced liver disease

- Advanced renal disease (dialysis patients)

- Aspirin sensitivity

- Autoimmune diseases

- Biological bioprosthesis valves

- Non-compliant & Drop out patient

- Pregnant women

- Caucasians.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Prevention


Related Conditions & MeSH terms

  • Complications Due to Heart Valve Prosthesis

Intervention

Drug:
Acetyl Salicylic Acid

Warfarin

Placebo (for Aspirin)
Sugar pill manufactured to mimic 75 mg Aspirin

Locations

Country Name City State
Egypt Ain Shams University hospitals Cairo

Sponsors (1)

Lead Sponsor Collaborator
Pharmacoeconomic Unit, Egypt

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Mohamed H. Antithrombotic therapy in patients with prosthetic heart valves. Libyan J Med. 2009 Mar 1;4(1):54-6. doi: 10.4176/090115. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Valve Thrombosis one year No
Secondary Major Systemic Embolism, one year No
Secondary Non-fatal intracranial hemorrhage one year Yes
Secondary Major extra cranial hemorrhage, one year Yes