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The Effect of Some Parturients' Characteristics on Sensory Block Level After Spinal Anesthesia

The Effect of Body Mass Index, Intra-abdominal Pressure, Abdominal Girth and Waist Circumference on Sensory Block Level After Single-shot Spinal Anesthesia for Cesarean Section

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03164096
Enrollment
100
Registered
2017-05-23
Start date
2017-06-01
Completion date
2018-12-10
Last updated
2018-03-29

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

Conditions

Anesthesia, Obstetrical

Brief summary

Although the exact mechanism remains unknown, the association of pregnancy and decreased local anesthetic requirement is clear. demonstrated that more local anesthetic is required for cesarean section under combined spinal-epidural anesthesia in preterm compared with term patients.

Detailed description

However, in pregnant patients, venous engorgement is prominent in the supine but not the lateral position, which suggests direct compression of the inferior vena cava by the gravid uterus. Second, an increase in intraabdominal pressure may affect the retroperitoneal area and may cause inward movement of soft tissue in the intervertebral foramina. Recent magnetic resonance imaging studies in pregnant patients, although without intraabdominal pressure measurements, suggested the latter because they showed limited contact of engorged veins along the dural sac which may therefore not be responsible for compression of the dura. If elevated intraabdominal pressure contributes to high anesthetic spread during pregnancy, one would expect a relationship between intraabdominal pressure and maximum sensory block level.

Interventions

DRUGBupivacaine Hydrochloride

intrathecal bupivacaine will be used for spinal anesthesia in obstetric patients undergoing C-section

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Intervention model description

evaluating relationship of sensory level and other patient factors

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* adult female partner * aged 18 to 40 years. * scheduled for elective cesarean section.

Exclusion criteria

* Patients with coagulopathy or under anti-coagulation therapy. * Gastrointestinal disease, * motion sickness. * diabetes mellitus. * Patients with preeclampsia,

Design outcomes

Primary

MeasureTime frameDescription
sensory levelfrom allocation until 24 hours post-operativeeffect of different parameters in sensory level
motor blockfrom allocation until 24 hours post-operativeeffect of different parameters in motor level

Secondary

MeasureTime frameDescription
hypotensionfrom allocation until 24 hours post-operativeincidence of hypotension after spinal anesthesia
vasopressor consumptionfrom allocation until 24 hours post-operativetotal dose of ephedrine consumed by the patients

Countries

Egypt

Outcome results

None listed

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