Overview
Chlorthalidone is a thiazide-like diuretic used for the treatment of hypertension and for management of edema caused by conditions such as heart failure or renal impairment. Chlorthalidone improves blood pressure and swelling by preventing water absorption from the kidneys through inhibition of the Na+/Cl− symporter in the distal convoluted tubule cells in the kidney. The exact mechanism of chlorthalidone's anti-hypertensive effect is under debate, however, it is thought that increased diuresis results in decreased plasma and extracellular fluid volume, decreased cardiac output and therefore overall reduction in blood pressure. Chlorthalidone is considered first-line therapy for management of uncomplicated hypertension as there is strong evidence from meta-analyses that thiazide diuretics such as chlorthalidone reduce the risk of stroke, myocardial infarction, heart failure, and cardiovascular all-cause mortality in patients with hypertension. In particular, the ALLHAT trial confirmed the role of thiazide diuretics as first-line therapy and demonstrated that chlorthalidone had a statistically significant lower incidence of stroke and heart failure when compared to Lisinopril, Amlodipine, or Doxazosin. Further studies have indicated that low-dose thiazides are as good as, and in some secondary endpoints, better than β-blockers, ACE inhibitors, Calcium Channel Blockers or ARBs. Chlorthalidone has been shown to have a number of pleiotropic effects that differentiate it from other diuretics such as Hydrochlorothiazide. In addition to its antihypertensive effects, chlorthalidone has also been shown to decrease platelet aggregation and vascular permeability, as well as promote angiogenesis in vitro, which is thought to be partly the result of reductions in carbonic anhydrase–dependent pathways. These pathways may play a role in chlorthalidone's cardiovascular risk reduction effects.
Background
Chlorthalidone is a thiazide-like diuretic used for the treatment of hypertension and for management of edema caused by conditions such as heart failure or renal impairment. Chlorthalidone improves blood pressure and swelling by preventing water absorption from the kidneys through inhibition of the Na+/Cl− symporter in the distal convoluted tubule cells in the kidney. The exact mechanism of chlorthalidone's anti-hypertensive effect is under debate, however, it is thought that increased diuresis results in decreased plasma and extracellular fluid volume, decreased cardiac output and therefore overall reduction in blood pressure. Chlorthalidone is considered first-line therapy for management of uncomplicated hypertension as there is strong evidence from meta-analyses that thiazide diuretics such as chlorthalidone reduce the risk of stroke, myocardial infarction, heart failure, and cardiovascular all-cause mortality in patients with hypertension. In particular, the ALLHAT trial confirmed the role of thiazide diuretics as first-line therapy and demonstrated that chlorthalidone had a statistically significant lower incidence of stroke and heart failure when compared to Lisinopril, Amlodipine, or Doxazosin. Further studies have indicated that low-dose thiazides are as good as, and in some secondary endpoints, better than β-blockers, ACE inhibitors, Calcium Channel Blockers or ARBs. Chlorthalidone has been shown to have a number of pleiotropic effects that differentiate it from other diuretics such as Hydrochlorothiazide. In addition to its antihypertensive effects, chlorthalidone has also been shown to decrease platelet aggregation and vascular permeability, as well as promote angiogenesis in vitro, which is thought to be partly the result of reductions in carbonic anhydrase–dependent pathways. These pathways may play a role in chlorthalidone's cardiovascular risk reduction effects.
Indication
Chlorthalidone is indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effect of other antihypertensive drugs in the more severe forms of hypertension. Chlorthalidone is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Chlorthalidone has also been found useful in edema due to various forms of renal dysfunction, such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure.
Associated Conditions
- Calcium Nephrolithiasis
- Edema
- Hypertension
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/03/01 | Early Phase 1 | Not yet recruiting | |||
2023/11/01 | Phase 2 | Recruiting | |||
2023/08/04 | Not Applicable | Not yet recruiting | |||
2023/06/22 | Phase 4 | Suspended | |||
2022/10/25 | Phase 4 | Recruiting | |||
2022/06/09 | Phase 4 | Completed | |||
2022/05/11 | Phase 2 | Active, not recruiting | |||
2022/03/11 | Phase 4 | Withdrawn | |||
2022/02/03 | Phase 2 | Recruiting | Indiana Institute for Medical Research | ||
2021/10/22 | Phase 1 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
A-S Medication Solutions | 50090-3910 | ORAL | 25 mg in 1 1 | 4/3/2018 | |
Zydus Pharmaceuticals USA Inc. | 68382-971 | ORAL | 50 mg in 1 1 | 10/5/2022 | |
Aidarex Pharmaceuticals LLC | 33261-942 | ORAL | 25 mg in 1 1 | 11/22/2013 | |
Aphena Pharma Solutions - Tennessee, LLC | 71610-029 | ORAL | 25 mg in 1 1 | 8/3/2021 | |
REMEDYREPACK INC. | 70518-3718 | ORAL | 25 mg in 1 1 | 3/28/2024 | |
Physicians Total Care, Inc. | 54868-2683 | ORAL | 25 mg in 1 1 | 7/9/2010 | |
Northwind Pharmaceuticals | 51655-790 | ORAL | 25 mg in 1 1 | 1/1/2023 | |
Actavis Pharma, Inc. | 0591-5782 | ORAL | 25 mg in 1 1 | 3/29/2024 | |
Direct_Rx | 72189-507 | ORAL | 25 mg in 1 1 | 9/20/2023 | |
JUBILANT CADISTA PHARMACEUTICALS,INC. | 59746-761 | ORAL | 50 mg in 1 1 | 2/24/2022 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
Chlortalidone Tablets | 国药准字H41020742 | 化学药品 | 片剂 | 6/17/2020 | |
Chlortalidone Tablets | 国药准字H51022786 | 化学药品 | 片剂 | 6/28/2020 | |
Chlortalidone Tablets | 国药准字H14022293 | 化学药品 | 片剂 | 4/20/2020 | |
Chlortalidone Tablets | 国药准字H11020601 | 化学药品 | 片剂 | 11/20/2020 | |
Chlortalidone Tablets | 国药准字H41025378 | 化学药品 | 片剂 | 9/4/2020 | |
Chlortalidone Tablets | 国药准字H51022815 | 化学药品 | 片剂 | 7/13/2020 | |
Chlortalidone Tablets | 国药准字H11020602 | 化学药品 | 片剂 | 11/20/2020 | |
Chlortalidone Tablets | 国药准字H41020760 | 化学药品 | 片剂 | 7/23/2020 |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
HYGROTON 25 chlortalidone 25mg tablet bottle | 11035 | Medicine | A | 8/2/1991 |