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The safety and comfort of early mobilisation following day case coronary angiography

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN74484491
Enrollment
Unknown
Registered
2006-09-29
Start date
2004-11-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Surgery: Coronary angiography Surgery Coronary angiography

Interventions

Randomisation of patients to either control or experimental group. Control group will mobilise at 4 hours (current practice) experimental group will mobilise at 1.5 hours. Other than ambulation time,

Sponsors

Record Provided by the NHSTCT Register - 2006 Update - Department of Health
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients able to attend for day case angiography.

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
1. Haematoma size 2. Complication rate: pseudoaneurysm, presence of bleeding.—

Secondary

MeasureTime frame
Not provided at time of registration—

Countries

United Kingdom

Outcome results

None listed

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