Comparison of ketamine /propofol Versus ketamine/Thiopental in Procedural Sedational analgesia for Reduction of Anterior Shoulder Dislocatio

Phase 3

Recruiting

Conditions: Procedural Sedational analgesia for Reduction of Anterior Shoulder Dislocation.
Subluxation and dislocation of shoulder joint
S43.0

Registration Number: IRCT20200809048341N1

Lead Sponsor: Yazd University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 90

Inclusion Criteria

Healthy patients without previous disease and those with mild systemic disease without functional limitations according to the American Society of Anesthesiologist classification (individuals 1 and 2)
Those who have been NPOs ( Nil Per Os) or consumed fluids in the last 3 hours
Those that do not need to be reduced in the operating room.
Age 18 to 64 years

Exclusion Criteria

Any contraindications including asthma and COPD(chronic obstructive pulmonary disease), systolic blood pressure below 90 or above 180, ischemic heart disease or heart failure, any symptoms in favor of increased intracranial pressure, glaucoma, psychosis and use of any psychotropic substances, acute or chronic alcoholism, liver or kidney failure, Allergies to any of the drugs studied or eggs or soy, people addicted to drugs, taking any sedatives or anesthetics before going to the emergency room, obstructive sleep apnea syndrome, maxillofacial malformations that block the airway, Pregnancy, dislocations lasting more than 24 hours, multiple trauma or hemodynamic instability, history of uncontrollable seizures, and patients who do not wish to participate in the study

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to appropriate sedation. Timepoint: 3 minutes after the last drug injection. Method of measurement: physical examination.;The duration of the effect of the drug. Timepoint: 15 minutes after drug injection. Method of measurement: Physical examination.;Discharge time. Timepoint: 15 minutes after drug infection. Method of measurement: Physical examination.;The pain before reduction. Timepoint: before starting reduction. Method of measurement: By the visual analog scale.;Need to additional doses of medication. Timepoint: 3 minutes after the last injection. Method of measurement: Physical examination.;Incidence of any side effects. Timepoint: Before injecting the drug and every 5 minutes. Method of measurement: Physical examination and vital signs.;Pain during reduction. Timepoint: During reduction. Method of measurement: By the facial pain scale.

Secondary Outcome Measures