UnknownPhase 4

Lignocaine Nebulization for Attenuation of Intubation Stress Response

Egypt100 participantsStarted 2021-02-24

Plain-language 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

Who can participate

Age range

18 Years – 45 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * American Society of Anesthesiologist (ASA) II , III with severe pre-eclampsia * Scheduled for caesarean deliveries under general anesthesia Exclusion Criteria: * severe obesity (BMI ≥ 40 ) * Cardiac patients * History of diabetes * Renal dysfunction (Elevated creatinine ≥ 2 mg\\dl) * Hepatic dysfunction (Elevated hepatic enzymes three times above normal value) * Known fetal anomalies

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Systolic, diastolic, mean arterial blood pressure

Timeframe: Preoperative-Intraoperative

Heart rate

Timeframe: Preoperative-Intraoperative

Peripheral oxygen saturation

Timeframe: Preoperative-Intraoperative

Cough score during emergence

Timeframe: Up to one hour after extubation

Trial details

NCT IDNCT04441073

SponsorAssiut University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-02-23

Contact for this trial

Fatma N. Mohamed, M.D.

+201003633992 fatmanabil2012@gmail.com

View on ClinicalTrials.gov More Pressor Response trials

Who can participate

Age range

18 Years – 45 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.