Clinical Trials Directory

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UnknownNCT04441073

Lignocaine Nebulization for Attenuation of Intubation Stress Response

Lignocaine Nebulization for Attenuation of Intubation Stress Response in Patients With Severe Pre-eclampsia: a Prospective Double-blinded Placebo-controlled Trial

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Assiut University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

To study the effect of lignocaine nebulization on attenuation of the pressor response during induction and emergence of anesthesia in patients with severe pre-eclampsia

Detailed description

The pressor response to laryngoscopy and tracheal intubation is a very important issue in hypertensive pregnant patients that can lead to increased maternal intracranial pressure, cerebral haemorrhage, and cardiac failure with pulmonary oedema and may result in maternal mortality. The catecholamine release associated with laryngoscopy and intubation also causes uteroplacental vasoconstriction and adversely affect the neonate well-being. Therefore, the precise control of stress is necessary during general anesthesia in pre-eclamptic patients.Various drugs are used to suppress the pressor response including opioids, lidocaine, along with α and β adrenergic blockers. in this study the investigators will evaluate the effect of lignocaine nebulization on attenuation of the pressor response.

Conditions

Interventions

TypeNameDescription
DRUGLignocainepreoperative nebulization of lignocaine
DRUGPlacebopreoperative nebulization of normal saline (Nacl 0.9%) as a placebo

Timeline

Start date
2021-02-24
Primary completion
2022-02-23
Completion
2022-02-23
First posted
2020-06-22
Last updated
2022-01-19

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04441073. Inclusion in this directory is not an endorsement.