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Influence of Maternal Postioning on Spread of Local Anesthetic After Epidural Analgesia

R

Region Skane

Status

Completed

Conditions

Effects of; Anesthesia, Spinal and Epidural, in Pregnancy

Treatments

Procedure: lateral position

Study type

Interventional

Funder types

Other

Identifiers

NCT02617823
SUSAN-KK

Details and patient eligibility

About

The purpose of this study is to determine if a lateral positioning of the pregnant woman after epidural analgesia increases the incidence of unilateral functioning epidurals.

Full description

Pregnant women requesting epidural analgesia will be randomized to either left lateral or semi-recumbent position for 30 minutes after the first epidural bolus-injection.

After 30 minutes, the clinical effect of the analgesia will be evaluated by an anesthesiologist if available or by a midwife if the anesthesiologist is unavailable. The study-period is concluded thereafter and further positioning is optional.

Maternal and fetal wellbeing are continuously being monitored during the study period and complications/interventions registered. APGAR and CTG results during the intervention will be registered and evaluated at a later stage.

Enrollment

950 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • all adult pregnant women recieiving epidural analgesia

Exclusion criteria

  • participation refused
  • inability to understand study purpose/instructions
  • study postition could not be maintained for 30 min
  • ineffective epidural

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

950 participants in 2 patient groups

semi-recumbent
No Intervention group
Description:
rutine positioning at the hospital today
lateral position
Experimental group
Description:
experimental position to be evaluated against rutine
Treatment:
Procedure: lateral position

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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