Evaluation of NEXFIN During Cesarean Delivery to Detect Hypotension (NEXFIN-CESAR)

Hopital Foch

Status: Completed

Conditions: Hypotension

Treatments: Device: Nexfin

Study type: Interventional

Funder types: Other

Identifiers

NCT01732133

2012/27

2012-A00811-42 (Other Identifier)

Details and patient eligibility

About

Hypotension after spinal anesthesia for cesarean delivery occurs frequently. Oscillometric measurement gives intermittent informations. Nexfin, a continuous noninvasive device, could help to detect hypotension.

Enrollment: 171 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• adult patients undergoing elective cesarean delivery performed under spinal anesthesia

Exclusion criteria

• patients with a heart rhythm disorder, Raynaud's disease or a history of vascular surgery of the upper limb

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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171 participants in 1 patient group

Measurement of arterial pressure

Experimental group

Treatment:

Device: Nexfin