Table 2.
Studies carried out with N-acetylcysteine in different clinical conditions.
Disease | Study Type | Dose | Treatment Type | Administration Routes |
References |
---|---|---|---|---|---|
Lung diseases | |||||
Chronic obstructive pulmonary disease | Clinical trial | 600 mg/day | 3 years | Oral | [51] |
Clinical trial | 600 mg/day | 3 years | Oral | [52] | |
Clinical trial NCT01136239 | 1200 mg/day | 1 year | Oral | [53] | |
Clinical trial ChiCTR-TRC-09000460 | 1200 mg/day | 1 year | Oral | [54] | |
Clinical trial NCT01599884 | 3600 mg/day | 8 weeks | Oral | [55] | |
Systematic review with meta-analysis |
>600 mg/day | Long term | Oral | [56] | |
Systematic review with meta-analysis |
≥1200 mg/day | Long term | Oral | [57] | |
Systematic review |
Low doses: ≤600 mg/day High doses: >600 mg/day |
Minimum of 6 months | Oral | [58] | |
Cystic fibrosis | Systematic review with meta-analysis |
600 mg to 2800 mg/day | 3.9 and 12 months | Oral or inhalation | [59] |
Clinical trial | 1800, 2400 and 3000 mg/day | 4 weeks | Oral | [60] | |
Clinical trial 2007-001401-15 |
2400 mg/day | 4 weeks | Oral | [61] | |
Idiopathic pulmonary fibrosis | Systematic review with meta-analysis |
704.8 to 1800 mg/day | - | Oral or inhalation | [62] |
Systematic review with meta-analysis |
Oral doses: 1800 mg/day Inhalation doses: 704.8 mg |
3 to 15 months | Oral or inhalation | [28] | |
Cardiovascular diseases | Clinical trial | 15,000 mg/day | 24 h | Intravenous | [63] |
Clinical trial | 15,000 mg/day | 24 h | Intravenous | [64] | |
Cardiac surgery | Systematic review with meta-analysis |
<100 mg/kg/ to ≥300 mg/kg/day |
<24 and >48 h | Oral and/ or intravenous | [65] |
Systematic review with meta-analysis |
50 mg/kg to 600 mg | Until 48 h | Oral and/ or intravenous | [66] | |
Clinical trial | 50–150 mg/kg | 1 h preoperatively and 48 h postoperatively | intravenous | [67] | |
Psychiatric illnesses | |||||
Schizophrenia | Multicenter clinical trial |
2000 mg/day | 4 weeks | Oral | [68] |
Clinical trial IRCT:2015080223463 | 1200 mg/day | 12 weeks | Oral | [69] | |
Systematic review with meta-analysis | 600 mg to 3600 mg/day | ≥24 weeks | Oral | [70] | |
Clinical trial NCT01354132 |
2700 mg/day | 6 months | Oral | [71] | |
Bipolar disorder | Clinical trial ACTRN12612000830897 | 2000 mg/day | 16 weeks | Oral | [72] |
Clinical trial 12605000362695 | 1000 mg/day | 24 weeks | Oral | [73] | |
Depression | Clinical trial ACTRN12607000134426 |
1000 mg/day | 12 weeks | Oral | [74] |
Systematic review with meta-analysis |
1000 mg to 3000 mg/day | - | Oral | [75] | |
Neurodegenerative diseases | |||||
Parkinson’s disease | Clinical trial NCT01427517 |
150 mg/kg | 1 h | Intravenous | [76] |
Clinical trial NCT02445651 |
Intravenous doses: 50 mg/kg Oral doses: 1000 mg/day |
3 months | Oral and intravenous | [77] | |
Clinical trial NCT02212678 |
6000 mg/day | 4 weeks | Oral | [78] | |
Alzheimer’s disease | Clinical trial NCT00903695 |
600 mg/day | 6 months | Oral | [79] |
Multiple sclerosis | Clinical trial NCT02804594 |
1250 mg/day | 4 weeks | Oral | [80] |
Clinical trial NCT03032601 |
Intravenous doses: 50 mg/kg (once a week) Oral doses: 1000 mg/day (6 times a week) |
2 months | Oral and Intravenous | [81] | |
Liver diseases | |||||
Paracetamol poisoning | Guide clinical practice | 200 mg/kg in 4 h, then 100 mg/kg in 16 h | 20 h | Intravenous | [82] |
Acute liver failure | Randomized case control study | 150 mg/kg over 1 h, followed by 12.5 mg/kg/h for 4 h and continuous infusion of 6.25 mg/kg/h for the remaining 67 h | 72 h | Intravenous | [83] |
Systematic review |
150 mg/ kg over 1 h, followed by 12.5 mg/kg/h for 4 h, and continuous infusions of 6.25 mg/kg/h for the remaining 67 h | 72 h | Intravenous | [84] | |
Nonalcoholic fatty liver disease | Clinical trial | 600 mg/day | 3 months | Oral | [85] |
Acute alcoholic hepatitis | Multicenter clinical trial NCT00863785 |
Day 1: at a dose of 150, 50, and 100 mg/kg a period of 30 min, 4 h, and 16 h, respectively; Days 2 through 5: 100 mg/kg | 28 days | Intravenous | [86] |
Multicenter clinical trial | 300 mg/kg | 14 days | Intravenous | [87] | |
Kidney diseases | |||||
Chronic renal patients undergoing cardiac | Systematic review with meta-analysis |
150 mg/kg to 1200 mg | 6 h to 7 days | Intravenous | [88] |
Chronic kidney disease | Clinical trial | 5000 mg | One hemodialysis session | Intravenous | [89] |
Clinical trial | 600 mg/day | 2 doses with 1 week interval | Oral | [90] | |
Gastrointestinal diseases | |||||
Helicobacter pylori infection | Clinical trial | 600 mg/day | 14 days | Oral | [91] |
Clinical trial | 800 mg/day | 5 days | Oral | [92] | |
Colon cancer associated with colitis | Systematic review |
8000 mg to 1200 mg/day | 7 days to 12 weeks | Oral | [93] |
Gastrointestinal cancer | Clinical trial | 1200 mg/day | 2 days before surgery until the fifth day postoperatively | Schematic parenteral | [94] |
Clinical trial | 800 mg/day | 12 weeks | Oral | [95] | |
Ulcerative colitis | Clinical trial | 800 mg/day | 4 weeks | Oral | [96] |
Infectious diseases | |||||
Chronic hepatitis B | Clinical trial | 8000 mg/day | 28 days | Intravenous | [97] |
Pulmonary tuberculosis | Clinical trial | 600 mg/day | 2 months | Oral | [98] |
SARS-CoV-2 | Clinical trial NCT04374461 |
6000 mg/day | 3 weeks | Intravenous | [99] |
Chorioamnionitis | Clinical trial | 100 mg/kg/dose and 12.5–25 mg/kg/dose their infants | Diagnosis until delivery and every 12 h for 5 doses to their infants | Intravenous | [100] |
Infection and/or intrauterine inflammation | Clinical trial NCT00397735 |
150 mg/kg administered in 1 h, followed by continuous infusion of NAC (50 mg/kg) for 4 h and infusion of 100 mg/kg of NAC in the next 16 h or until delivery | - | Intravenous | [101] |
Acute pyelonephritis | Clinical trial NCT02080182 |
Children with a body weight equal to or greater than 30 kg, 900 mg/day, children weighing between 8.5–30 kg, 600 mg/day, and those weighing less than 8.5 kg, 70 mg/kg/day | 5 days | Oral | [102] |
Cancer prevention and treatment | |||||
Radiation therapy, head and neck cancer | Prospective, controlled multicenter study | 2400 mg/day | 8 weeks | Inhalation therapy | [103] |
Clinical trial NCT02123511 |
2500 mg/day | - | Rinsing | [104] | |
Other conditions | |||||
Smoking cessation | Clinical trial NCT02420418 |
1800 mg/day | 12 weeks | Oral | [105] |
Male fertility | Clinical trial IRCT20170830035998N4 |
600 mg/day | 3 months | Oral | [106] |
Sickle cell anemia | Clinical trial NTR1013 |
1200 or 2400 mg/day | 6 weeks | Oral | [107] |
Clinical trial | 600 mg, 1200 mg or 2400 mg/day | 7 months | Oral | [108] | |
Pre-eclampsia | Clinical trial | 400 mg/day | 6 weeks | Oral | [109] |
Clinical trial | 600 mg/day | - | Oral | [110] | |
Metabolic syndrome | Pilot study | 1200 mg/day | 6 weeks | Oral | [111] |
Ocular condtions | |||||
Chronic blepharitis | Clinical trial | 100 mg/day | 1 to 4 months | Oral | [112] |
Meibomian gland dysfunction | Clinical trial | 5% | 1 month | Eye drops | [113] |
Clinical trial | 5% | 1 month | Eye drops | [114] |