Skip to content

Comparing the Association of continuation or discontinuation of Aspirin with bleeding volume during and after skin tumor surgery

Comparing the Association of continuation or discontinuation of Aspirin with bleeding volume during and after skin tumor surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201602049768N5
Enrollment
70
Registered
2016-02-17
Start date
2014-11-22
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

skin cancer. Other malignant neoplasms of skin Incl.: malignant neoplasm of: sebaceous glands sweat glands

Interventions

Intervention 1: 80 mg oral Aspirin for the intervention group. Intervention 2: Placebo in the control group.
Treatment - Drugs
Placebo
80 mg oral Aspirin for the intervention group

Sponsors

Vice chancellor of research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Adult patients who use Aspirin for at least 3 months, aged 40-75 years and INR between 1 and 1.5 Exclusion criteria: Dementia, movement disorders, simultaneous participation in another trial, severe life threatening cardiovascular disease (NYHA class III or more, history of myocardial infarction), valvular heart disease, bleeding disorders, use of other antiplatelet drugs or anticoagulants, history of gastrointestinal bleeding.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bleeding volume within and after surgery. Timepoint: during the operation and 24 hous afterwards. Method of measurement: weight of blood absorbed to the dressing gas.

Secondary

MeasureTime frame
Development of thrombosis. Timepoint: during surgery and 24 hous afterwards. Method of measurement: Clinical evaluation.;Hemodynamic unstability requiring reoperation. Timepoint: up to 24 hours from surgery. Method of measurement: Clinical evaluation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Arman Engheta

Tehran University of Medical Sciences, Razi Hospital.

A_ENGHETA@RAZI.TUMS.AC.IR+98 21 5560 9951

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 12, 2026