Thoracic Epidural Analgesia, Fracture Ribs Clinical Trial
Official title:
Comparative Study of Magnesium Sulfate Versus Fentanyl as Adjuvants to Bupivacaine for Thoracic Epidural Analgesia in Multiple Traumatic Fracture Ribs
This work aims at comparing the analgesic effect of Thoracic Epidural Magnesium sulfate versus Fentanyl when added as adjuvants to Bupivacaine in patients with multiple traumatic fracture ribs.
Status | Not yet recruiting |
Enrollment | 60 |
Est. completion date | August 2019 |
Est. primary completion date | July 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 16 Years to 75 Years |
Eligibility |
Inclusion Criteria: 1. Patients 16 years of age and greater 2. Non-intubated at the time of block placement 3. Traumatic Rib Fractures two or greater 4. Block must be done within 12-24 hours of presentation to the emergency room 5. ASA physical status: I-II Exclusion Criteria: 1. Patient refusal 2. BMI more than 30 kg/m2 3. Need for mechanical ventilation on admission 4. Hemodynamic instability 5. Haemothorax or Pneumothorax 6. Contraindications of performing blocks as coagulopathy, vertebral column deformities, local infection 7. Traumatic head injury 8. Allergy to local anesthetic agents |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Assiut University |
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Difference in Pain Scores (Visual Analogue pain scale) | Visual analog scale [VAS] is a measure of pain intensity. It is a continuous scale comprised of a horizontal or vertical scale usually 10 cm or 100 mm length. For pain intensity, the scale is most commonly anchored by "no pain" (score of 0) and "pain as bad as it could be" or "worst imaginable pain" (score of 100 [on 100-mm scale]. The pain visual analog scale is self completed by the respondent. The respondent is asked to place a line perpendicular to the VAS line at the point that represents their pain intensity. After the patient has marked, using a ruler, the score is determined by measuring the distance (mm) on the 10-cm line between the "no pain" anchor and the patient's mark. The scores can be from 0-100. A higher score indicates greater pain intensity. Based on the distribution of pain, the following cut points on the pain VAS have been recommended: No pain (0 -4 mm) Mild pain (5-44 mm) Moderate pain (45-74 mm) Severe pain (75-100 mm) |
48 hours | |
Secondary | Development of pulmonary complications: respiratory rate by breath per minute (need for mechanical ventilation) | By observing respiratory rate of patients using clinical assessment every 1 hour | 48 hours | |
Secondary | Assessment of parameters of adequate ventilation and oxygenation: PaO2/FIO2 ratio | by measuring O2 level in the blood using arterial blood gases every 3 hours | 48 hours | |
Secondary | Assessment of parameters of adequate ventilation and oxygenation: PaCO2 in mmHg | by measuring CO2 level in the blood using arterial blood gases every 3 hours | 48 hours | |
Secondary | Changes in heart rate (HR) by beats per minute | By monitoring patients heart rate every 1 hour | 48 hours | |
Secondary | changes in arterial blood pressure (ABP) by mmHg | By monitoring patients arterial blood pressure using non invasive arterial blood pressure monitoring every 1 hour | 48 hours |