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Randomised, double-blind, controlled study of combined spinal epidural (CSE) analgesia for labour with and without epidural volume extension (EVE).

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN21230935
Enrollment
Unknown
Registered
2004-09-30
Start date
2003-07-01
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

Pregnancy and Childbirth: Analgesia Pregnancy and Childbirth Single delivery by caesarean section

Interventions

As of 29/07/09 the status of this trial was changed to 'stopped'. This trial was never commenced. Not provided at time of registration.

Sponsors

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

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Not provided at time of registration

Exclusion criteria

Exclusion criteria: Does not match inclusion criteria

Design outcomes

Primary

MeasureTime frame
To improve our existing CSE labour analgesia, in terms of rapidity of onset of action and decreased motor block in the lower limbs allowing earlier ambulation.—

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