The effects of coenzyme Q10 supplementation on burn patients

Phase 3

Recruiting

• Conditions: burns.; Burn of unspecified body region, unspecified degree; T30.0

• Registration Number: IRCT20201129049534N3
• 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: 12 July 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Age 65-18 years
Accept informed consent by the patient or his mobile
Gastrointestinal tract with normal function
Has a burn above 20%
Proper fluid recovery in the first 24 hours and hemodynamic stability after 48 hours

Exclusion Criteria

• Patients who are hospitalized for less than 48 hours or do not have stable conditions to start oral or tube feeding.
• Dissatisfaction of the patient or family.
• Patients with cancer undergoing chemotherapy and cisplatin.
Patients receiving warfarin.
• Pregnancy
Severe and progressive septic shock or sepsis
Hypovolemic shock in the first 48 hours
Patients who are expected to die within one week of admission.
• Patients with a history of certain diseases such as congenital and immune disorders, cirrhosis and pancreatitis.

Study & Design

• Study Type: interventional
• Study Design: Not specified