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Effect of mgso4 on Oxygenation and Lung Mechanics in Morbidly Obese Patients During Bariatric Surgery

Effect of MgSo4 Infusion on Oxygenation and Lung Mechanics in Morbidly Obese Patients Undergoing Bariatric Surgery.A Randomized Clinical Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04769440
Enrollment
40
Registered
2021-02-24
Start date
2021-03-01
Completion date
2022-02-21
Last updated
2022-07-20

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

Conditions

Anesthesia

Keywords

mgso4, oxygenation, lung mechanics

Brief summary

The purpose of this trial is to study the effect of mgso4 infusion on oxygenation and lung mechanics in morbidly obese patients undergoing bariatric surgery

Detailed description

Background and objectives: morbidly obese patients are characterized by a high prevalence of restrictive lung disease. Respiratory mechanics are significantly altered in obesity. These changes are exacerbated with general anesthesia .Obesity also results in reduced lung and chest wall compliance ,increased lung resistance ,reduced oxygenation.MgSo4 is promising in managing several respiratory disorders.it cause smooth muscle relaxation and reduce airflow obstruction. The objective of this trial is to study the effect of mgso4 infusion on oxygenation and lung mechanics in morbidly obese patients undergoing bariatric surgery. the following will be recorded :intraoperative oxygenation,lung mechanics,MAP,HR,EtCO2,plateau and peak airway pressure,sedation score,serum mgso4 level,change in P/F ratio and dynamic lung compliance,respiratory rate postoperative

Interventions

mgso4 infusion will start 15 minutes after intubation , 30 mg/kg LBW of 10%mgso4 in 100 ml normal saline I.V ,over 30 minutes followed by 10 mg/kg LBW for 90 minutes

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients age between 21-60 years. * BMI more than 40kg/m2 * Patients with restrictive lung disease(FVC\>70%) * American society of Anesthesiologists(ASA) physical status II * No previous abdominal surgery * Scheduled for laparoscopic bariatric surgery not exceeding 3 hours.

Exclusion criteria

* Patient refusal to participate in the study * ASA physical status more than II * patients with heart failure * Kidney disease * Patients on antiarrhythmic drugs * Patients taking beta or calcium channel blockers * Allergy to study drugs * Patients with combined restrictive-obstructive lung disease

Design outcomes

Primary

MeasureTime frameDescription
Pao25 minutes after intubation to 90 minutes after starting drug infusionarterial oxygenation during surgery determined by Pao2
Pao2/FIO25 minutes after intubation to 90 minutes after starting drug infusionarterial oxygenation during surgery determined by Pao2/FIO2

Secondary

MeasureTime frameDescription
Static lung compliance5 minutes after intubation to 90 minutes after starting drug infusionwill be calculated as:tidal volume/(plateau pressure-positive end expiratory pressure)
mg sulphate levelOne hour postoperativelyserum mgso4 level
dead space5 minutes after intubation to 90 minutes after starting drug infusiondead space will be calculated as : Vd/Vt
Dynamic lung compliance5 minutes after intubation to 90 minutes after starting drug infusionwill be calculated as :tidal volume/(peak airway pressure-positive end expiratory pressure)

Countries

Egypt

Outcome results

None listed

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