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Perioperative management of antiplatelet agents in general and visceral surgery: a pilot study

Pilot phase of a randomised controlled trial to optimise the perioperative management of antiplatelet agents in the field of general and visceral surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN45810007
Enrollment
50
Registered
2009-11-03
Start date
2009-01-01
Completion date
Unknown
Last updated
2022-11-07

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

Conditions

Surgical complication rates, thromboembolic events Not Applicable

Interventions

In the pilot phase, we provide low-risk patients with acetylsalicylic acid (ASA) 100 mg/day. There are two arms of randomisation: discontinuation versus continuation of aspirin. Patients stop 5 days b

Sponsors

University Hospital Heidelberg (Universitätsklinikum Heidelberg) (Germany)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Cardiac low and medium risk patients with antiplatelet agents 2. Informed consent 3. Aged over 18 years, either sex 4. Physical and psycological ability to participate in the trial

Exclusion criteria

Exclusion criteria: 1. Cardiac high risk patients 2. Psychiatric disorder 3. No informed consent

Design outcomes

Primary

MeasureTime frame
1. Bleeding complications 2. Thromboembolic events

Secondary

MeasureTime frame
1. Duration of surgery 2. Blood loss during surgery 3. Complication rate 4. Length of hospital stay 5. Readmission to hospital after discharge 6. Difference between laparoscopic versus open surgery

Countries

Germany

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 29, 2026