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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05322447
Other study ID # R / 2022
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date April 15, 2022
Est. completion date October 1, 2022

Study information

Verified date October 2022
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

L-Carnitine supplementation has been shown to boost muscular performance in several studies. In hemodialysis patients with muscular weakness, fatigue, or cramps/aches, after L-carnitine treatment, about two-thirds of patients had at least some improvement in muscular symptoms . L-Carnitine was also found to improve the left ventricular ejection fraction (LVEF) in hemodialysis patients with cardiac morbidity who had significantly reduced LVEF in echocardiography before supplementation. Moreover, L-Carnitine has been shown to improve muscular function and exercise performance in athletes in several studies


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date October 1, 2022
Est. primary completion date August 4, 2022
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - Age from 21 years old or greater - Both genders have respiratory failure either of the primary medical origin or in the post-surgical course. - Not in need of mechanical ventilation Exclusion Criteria: - Renal failure on regular dialysis - Hypothyroidism - Seizures - End-stage liver disease - Mechanical ventilation - History or discovered allergy to L-carnitine, pivampicillin, and other pivalate-conjugated antibiotics.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
L Carnitine ( low dose)
will receive a maintenance dose of L- carnitine 6 gm/day to keep normal level (normal L-carnitine level is normal 25-50 mmol/L)
L-Carnitine ( high dose)
will receive a high dose of L- Carnitine 18 gm/day as a continuous intravenous infusion to reach double the normal plasma level

Locations

Country Name City State
Egypt Faculty of medicine Cairo
Egypt Mona A Ammar Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ultrasound diaphragmatic function Diaphragmatic excursion by ultrasound at days 7
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