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Serial album for correct positioning during anesthesia during cesarean sections: clinical study

Educational tchnology for the correct positioning in Spinal Anesthesia: controlled and randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3z7srd
Enrollment
Unknown
Registered
2018-11-19
Start date
2017-06-12
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Spinal anesthesia

Interventions

Group 1: All pregnant in group 1 will receive the preoperative guidelines on positioning for routine spinal anesthesia of the service. Group 2: All pregnant in group 2 will receive the preoperative g
Other

Sponsors

Universidade Regional do Cariri
Lead Sponsor
Universidade Federal do Ceará
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Pregnant aged 18 or over; With indication of cesarean section of gestation topical; with single fetus

Exclusion criteria

Exclusion criteria: Pregnant women who evolve with clinical or obstetric complications, who present some difficulty in understanding and verbal expression that prevents them from participating in the educational intervention or from responding to the instruments of data collection

Design outcomes

Primary

MeasureTime frame
Presentation of correct positioning of pregnant women during spinal anesthesia; increased presentation of at least 70% of the characteristics necessary for correct positioning (immobility, relaxed shoulders, spine flexion)

Secondary

MeasureTime frame
Amount of lumbar puncture until obtaining successful puncture; obtained by observation of the lumbar puncture procedure; waiting for reduction to the maximum number of 2 puncture attempts to obtain a successful procedure.

Countries

Brazil

Contacts

Public ContactSarah Pinto

Universidade Regional do Cariri

sarahlimapinto@gmail.com+55-088-988227400

Outcome results

None listed

Source: REBEC (via WHO ICTRP)