Magnesium Sulfate in Surgical Stress Attenuation Postoperative Sore Throat and Stress Response Induced Tracheal Intubation

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06091631
Collaborator
(none)
100
2
9

Study Details

Study Description

Brief Summary

Magnesium sulfate has many mechanisms of action for attenuating the stress response as inhibition of catecholamine releasing from the adrenal medulla, keeping the plasma concentration of epinephrine at a fixed level, decreasing the circulating norepinephrine level when compared to that of a control group[ and also has a vasodilation effect on systemic and coronary blood vessels by blocking calcium ion in vascular smooth muscle.-Methyl- D-Aspartate (NMDA) antagonism is an amazing recent discovery for magnesium sulphate to play an important role in stress response.

In this study, we will study the effects of nebulized magnesium sulfate on hemodynamics during intubation.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Magnesium sulfate vaporization
N/A

Detailed Description

Inclusion criteria

  • 20-50 years old

  • ASA: 1, 2

  • Elective fit laparoscopic cholecystectomy Exclusion criteria

  • Patient refusal

  • patients with history of hypersensitivity to magnesium sulphate

  • patients with coronary ischemic disease, atrioventricular block of any degree, known cardiac arrhythmias, heart failure

  • on beta blockers or calcium channel blockers

  • expected difficult intubation (Mallampati 4)

  • Body mass index > 40

Study tools:

Following institutional ethical committee approval and written informed consent,a prospective randomized double-blinded study. After written informed consent wil be given, 100 patients, ASA 1 or 2, aged between 20 - 50 years, scheduled for elective surgery with Orotracheal Intubation (OTI) will be assessed for eligibility. Patients will be recruited in the study divided into two equal groups; Patients in Group A: will receive nebulized magnesium sulfate in 3 ml (240 mg) over 15 min, While group B: will receive nebulized normal saline in 3 ml over 15 min, ending 5 min before the induction of anesthesia. SBP, DBP, HR, and blood glucose level will be measured at the following intervals; Baseline (before induction), after premedication (sedation), after induction, after ETT intubation, 3 min later, 6 min later.

Full monitoring data (Blood pressure every 3 minutes, ECG, Nanogram, and pulse oximeter) wil be collected till 6 minutes then every 5 minutes. Random blood sugar will be tested 5 minutes pre-intubation, 3minutes and 5 minutes after intubation.

After end of nebulization, sedation with 2 mg midazolam and IV fluids (10 ml/kg) will be infused to avoid tachycardia of dehydration and fear of surgery. Then, we proceed on general anesthesia through propool titration + fentanyl 100 mcg + Cisatracurium 0.15 mg/kg. Endotracheal intubation with cuffed tube and mechanical ventilation with mild increase in respiratory rate 14-16/min to overcome CO2 peritoneal insufflation. All patients will receive intraoperatively, nalbuphine 0.1 mg/kg + ketorolac 60 mg + paracetamol IV 1 g. Dexamethasone 4mg + Ondansetron 4mg will be received to all patients for prophylaxis against postoperative nausea and vomiting. After end of surgery, cessation of inhalational anesthesia and reversal of muscle relaxation with neostigmine 2.5 mg+ Atropine 1mg will be done.

Consumption of isoflurane intraoperatively will be recorded. Post operative assessment for pain using VAS score will be assessed 2 hours after recovery.

Time for recovery after stop of isoflurane will be estimated.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
2 groups are investigated. Each group consists of 50 patients. First group will receive magnesium sulfate inhalation . The other group will receive distilled water inhation2 groups are investigated. Each group consists of 50 patients. First group will receive magnesium sulfate inhalation . The other group will receive distilled water inhation
Masking:
Single (Participant)
Masking Description:
the participant will not know whither a magnesium sulfate inhalation or distilled water in the vaporizer
Primary Purpose:
Other
Official Title:
Effect of Magnesium Sulfate Nebulization on Postoperative Sore Throat and Stress Response Induced Tracheal Intubation
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Aug 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Magnesium sulfate

will receive magnesium sulfate inhation

Procedure: Magnesium sulfate vaporization
pre-opeative magnesium sulfate vaporization

No Intervention: Control

Will receive distilled water vaporization

Outcome Measures

Primary Outcome Measures

  1. Incidence of post-operative sore throat at 0 hours in both groups [at 0 hours in both groups]

    Incidence of post-operative sore throat 0 h

  2. Incidence of post-operative sore throat at 2 hours in both groups [at 2 hours in both groups]

    Incidence of post-operative sore throat 2 h

  3. Incidence of post-operative sore throat at 4 hours in both groups [at 4 hours in both groups]

    Incidence of post-operative sore throat 4 h

  4. Incidence of post-operative sore throat at 24 hours in both groups [at 24 hours in both groups]

    Incidence of post-operative sore throat 24 h

Secondary Outcome Measures

  1. Improvement in postoperative stress response after (3, 6) minutes including: • Heart rate > 20% baseline • Systolic and mean BP >25% baseline • Random blood sugar increase > 50 mg/dl from baseline [(3, 6) minutes]

    Improvement in postoperative stress response after (3, 6) minutes including: Heart rate > 20% baseline Systolic and mean BP >25% baseline Random blood sugar increase > 50 mg/dl from baseline

  2. Effect on Pain score VAS 2hours after recovery [2hours after recovery]

    Effect on Pain score VAS visual analogue scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 20-50 years old

  • ASA: 1, 2

  • Elective fit laparoscopic cholecystectomy

Exclusion Criteria:
  • -Patient refusal

  • patients with history of hypersensitivity to magnesium sulphate

  • patients with coronary ischemic disease, atrioventricular block of any degree, known cardiac arrhythmias, heart failure

  • on beta blockers or calcium channel blockers

  • expected difficult intubation (Mallampati 4)

  • Body mass index > 40

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ayman Abd El-Khalek Mohammed Glala, principal investigator, Assiut University
ClinicalTrials.gov Identifier:
NCT06091631
Other Study ID Numbers:
  • Attenuation of surgical stress
First Posted:
Oct 19, 2023
Last Update Posted:
Oct 19, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ayman Abd El-Khalek Mohammed Glala, principal investigator, Assiut University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 19, 2023