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An investigation to compare analgesia from 0.5 mg or 1 mg of intrathecal diamorphine when undergoing total knee replacement surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN28694723
Enrollment
Unknown
Registered
2004-09-30
Start date
2003-03-10
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

Total knee replacement (TKR) surgery analgesia Surgery Surgery analgesia

Interventions

Prior to total knee replacement surgery, patients will be randomised to: 1. 0.5 mg intrathecal diamorphine 2. 1 mg intrathecal diamorphine

Sponsors

Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult primary total knee replacements 2. Aged 18 - 70 years

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Not provided at time of registration—

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