The effectiveness of Bupivacaine administration to control the pain of chest tube

Phase 2

Recruiting

• Conditions: Rib fractures.; Multiple fractures of ribs; S22.4

• Registration Number: IRCT20120716010297N6
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 April 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 32

Inclusion Criteria

Traumatic patients with rib fractures
ABG3 abnormality
Consent to participate in the study
If there is pentothorax and hemothorax for the patient.

Exclusion Criteria

The patient is drug addicted
The patient's blood pressure is less than 90/60 mmHg or greater than 180/110 mmHg that may cause the patient to require any further intervention
The patient has unstable conditions and needs further action
Need for intubation in patients
Being allergic to bupivacaine

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The amount of prescribed opioid analgesic medication. Timepoint: During the intervention. Method of measurement: Patient's records.;HCO3. Timepoint: Before the intervention and every 0.5 hours to 4 hours after the intervention. Method of measurement: blood test.;PO2. Timepoint: Before the intervention and every 0.5 hours to 4 hours after the intervention. Method of measurement: blood test.;PCO2. Timepoint: Before the intervention and every 0.5 hours to 4 hours after the intervention. Method of measurement: blood test.;Pain. Timepoint: Before the intervention and every 10 minutes to 4 hours after the intervention. Method of measurement: visual analogue scale.