Determining the effect of venous magnesium on improving the quality of anesthesia

Early Phase 1

Recruiting

Conditions: Condition 1: Appendicitis. Condition 2: pain. Condition 3: nausea and vomiting.
Acute appendicitis
Pain, unspecified
Nausea and vomiting

Registration Number: IRCT20230307057651N1

Lead Sponsor: Ardabil University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 84

Inclusion Criteria

Age 18 to 50 years, acute appendicitis patients

Exclusion Criteria

History of drug abuse, alcohol consumption, recent use of tranquilizers, stimulants and antipsychotics, antihypertensive drugs, calcium channel blockers, and history of neuromuscular diseases, thyroid disorders, history of any type of kidney and heart disease.

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Pain measurement at 1, 3, 6, 12 and 18 hours after surgery. Method of measurement: The measurement of patients' pain will be based on the criteria for measuring patients pain with 'Visual Analogue Scale.Zero point is equal to not having any pain and 10 is the most severe possible pain.

Secondary Outcome Measures

Name	Time	Method
ausea and vomiting. Timepoint: 3 and 12 hours after surgery. Method of measurement: Based on a qualitative review by the following method:1- No nausea and vomiting 2- Nausea 3- Nausea and vomiting one to two times 4- Nausea and vomiting more than 2 times.;Anxiety and restlessness. Timepoint: 3, 6, 12, 18 hours after surgery. Method of measurement: According to Ramsey scale (0 to 5): 0 (restless), 1 (calm and alert), 2 (sleepy), 3 (confused but responding to verbal commands), 4 (no response to verbal commands), 5 (absence) response to provocations)).;Consent of the surgeon. Timepoint: During surgery. Method of measurement: has / does not have.