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A Study on the Effect of Position on Walking Labour Epidural Efficacy

Which Position is Best: A Randomized Clinical Trial on the Effect That Position Has on Walking Labour Epidural Analgesia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04469101
Enrollment
216
Registered
2020-07-13
Start date
2021-05-31
Completion date
2022-10-31
Last updated
2021-10-18

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

Conditions

Analgesia, Epidural, Labor Pain

Keywords

Analgesia, Obstetrical, Posture, Pregnancy, Female, Heart Rate, Fetal, Hypotension

Brief summary

This study is being done to better understand how patient positioning can affect pain relief after an epidural. In addition to pain, the investigators will assess how position affects epidural spread, and its effects on maternal blood pressure and fetal heart rate.

Detailed description

Epidurals will be placed with parturients in the standard sitting position. An epidural catheter will be placed to a depth of 5 cm into the epidural space. After placement, parturients will be randomized to one of the four position groups (left uterine displacement, left lateral, right lateral, or seated upright). After successful positioning, a series of 5 cc bolus doses of 0.08% ropivacaine with 2 mcg per cc of fentanyl will be injected through the epidural catheter in 5 minute intervals for a total volume of 20 cc. After the initial loading dose of epidural solution has been injected in the first 20 minutes post-insertion, the patient will be able to return to whatever position they are most comfortable with. The parturient will be asked to rate their pain on a verbal pain scale of between 0 and 10 at the peak of their contraction at three time intervals. The spread of the blockade will be assessed with ice applied along both the left and right mid-clavicular lines. Maternal blood pressure will be measured on the upper arm in all patients as per nursing protocol. Fetal heart rate will be monitored intermittently with Doppler ultrasound as per nursing protocol.

Interventions

Parturients will have an epidural placed in the upright seated position as per institution standard. After epidural placement, they will be positioned as per their randomization. They will then have a total of 20 cc of epidural solution (0.08% ropivacaine with 2 mcg per cc of fentanyl) injected into the epidural in boluses of 5 cc every 5 minutes.

Sponsors

University of Saskatchewan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Active labour or admitted for induction of labour * Requesting an epidural for labour analgesia * Contractions occurring greater than once every 5 minutes

Exclusion criteria

* Coagulation disorder * High risk pregnancy as per obstetrics * Spinal pathology (included scoliosis, herniated disks, or previous lumbar back surgery)

Design outcomes

Primary

MeasureTime frameDescription
Labour pain based on verbal rating pain scaleTaken at time 0 minutes after epidural insertionPain with contractions, assessed using a 0 to 10 verbal rating pain scale; 0 being no pain with a contraction and 10 being the worse pain with a contraction.

Secondary

MeasureTime frameDescription
Assessment of epidural levels based on dermatomesTaken at time 20 minutes after epidural insertionLevels of analgesia assessed via temperature insensitivity to ice on the right and left side along the midclavicular lines of the patient and reported as dermatome levels.
Category of epidural based on bilateral dermatome levelsTaken at time 20 minutes after epidural insertionEpidural assessed if it is successful, unilateral (more than two dermatome level difference between sides), patchy (one or more areas between dermatomes that remain sensitive to temperature assessment), or failed (no measurable dermatome levels) based on the dermatome levels gathered by nursing assessments.
Events of maternal hypotension after epidural placementBlood pressure taken with a non-invasive blood pressure monitoring cuff every 5 minutes for 20 minutes after epidural insertionHypotensive events defined as a deviation of greater than 20% of maternal blood pressure compared to pre-epidural baseline.
Events of fetal bradycardia after epidural placementIntermittent fetal heart rate monitoring via doppler as per nursing protocol for 20 minutes after epidural insertionFetal bradycardic events defined as a fetal heart rate of less than 120 bpm after epidural placement.

Countries

Canada

Contacts

Primary ContactMonica San Vicente, MD
mks773@mail.usask.ca306-655-1183
Backup ContactAlex Stathakis, MD
alex.stathakis@usask.ca902-456-0391

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026