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Reliability of Ultrasound Assisted Epidural Analgesia in Obese and Normal Weight Parturients

Reliability of Ultrasound Assisted Epidural Analgesia in Obese and Normal Weight Parturients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01438099
Enrollment
300
Registered
2011-09-21
Start date
2011-10-31
Completion date
2013-07-31
Last updated
2013-08-26

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

Conditions

Pregnancy

Keywords

epidural analgesia, ultrasound, labor analgesia, labor

Brief summary

This study wants to investigate if ultrasound assisted epidural catheter insertion for labor analgesia is easier and safer to the standard epidural technique.

Detailed description

This study has four specific aims: 1. to evaluate congruity between palpatory technique and ultrasound lumbar evaluation to identify the correct spinal space; 2. to compare between ultrasound evaluation and needle measure of skin-epidural space depth; 3. to compare between longitudinal and transverse ultrasound epidural space depth in obese and normal parturients; 4. to check the reduction of complications and failure rates of epidural analgesia with ultrasound assistance.

Interventions

None listed

Sponsors

Università degli Studi dell'Insubria
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* all women who request epidural analgesia for labor

Exclusion criteria

* all women who present contraindication for epidural analgesia

Design outcomes

Primary

MeasureTime frameDescription
The congruity between palpatory technique and ultrasound lumbar evaluationparticipants will be followed for the duration of hospital stay, an expected average of 3 daysThe congruity between palpatory technique and ultrasound lumbar evaluation to identify the correct spinal space performing epidural analgesia

Secondary

MeasureTime frameDescription
Longitudinal and transverse ultrasound epidural space depth in obese and normal parturientsparticipants will be followed for the duration of hospital stay, an expected average of 3 daysLongitudinal and transverse ultrasound epidural space depth in obese and normal parturients will be measured and compared to the needle depth

Countries

Italy

Outcome results

None listed

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