Title:
Protocol and Methods: Role of Levothyroxine on the Progression of Chronic Kidney Disease in Subclinical Hypothyroid Populations (LP‑CKD) – A Multicenter Randomized Controlled Trial

dc.contributor.authorNarayan Prasad
dc.contributor.authorShivendra Singh
dc.contributor.authorVivek Kumar
dc.contributor.authorManisha Sahay
dc.contributor.authorArpita Ray Chaudhury
dc.contributor.authorManas Ranjan Behera
dc.contributor.authorRavi Shankar Kushwaha
dc.contributor.authorDeependra Yadav
dc.contributor.authorSonam Gautam
dc.contributor.authorAkhilesh Jaiswal
dc.date.accessioned2026-02-07T11:36:30Z
dc.date.issued2023
dc.description.abstractIntroduction: Subclinical hypothyroidism (SCH) is highly prevalent and associated with chronic kidney disease (CKD). However, it is still unanswered whether the restoration of euthyroid status in these patients will be beneficial in retarding a decline in glomerular filtration rate in early CKD patients. We aim to evaluate the efficacy of levothyroxine therapy versus placebo in slowing estimated glomerular filtration rate (eGFR) decline among CKD patients (stage 2–4) with SCH. Methods: This study will be a multicentric, double‑blind, randomized, parallel‑group, placebo‑controlled study. A total of 500 CKD patients, 250 patients in the treatment group and 250 patients in the placebo group, will be randomized. The randomization between the treatment arm and placebo arm will be performed as per the computer‑generated random number table in a 1:1 ratio. The sample size was calculated based on the assumed reduction in eGFR after 1‑year follow‑up in the treatment and placebo groups of 10% and 25%, respectively, at a minimum two‑sided 99% confidence interval and 90% power of the study and considering 20% loss on follow‑up. Each patient will be followed every 3 months for at least 1 year after randomization. Individuals completing 1‑year follow‑up visits will be considered for analysis. The baseline and follow‑up data will be compared between the treatment and placebo groups. The study will evaluate the efficacy and safety of levothyroxine therapy versus placebo in slowing eGFR decline among CKD patients (stage 2‑4) with SCH. The primary endpoint will be the end of follow‑up of the patients, reduction of eGFR by ≥50% from a baseline of that patient, or development of ESKD or death of the patients. The secondary endpoint will be any cardiovascular event or arrhythmia after the institution of the drug. © 2023 Wolters Kluwer Medknow Publications. All rights reserved.
dc.identifier.doi10.4103/ijn.ijn_188_22
dc.identifier.issn9714065
dc.identifier.urihttps://doi.org/10.4103/ijn.ijn_188_22
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/46059
dc.publisherWolters Kluwer Medknow Publications
dc.subjectChronic kidney disease progression
dc.subjectestimated glomerular filtration rate
dc.subjectlevothyroxine
dc.subjectsubclinical hypothyroidism
dc.titleProtocol and Methods: Role of Levothyroxine on the Progression of Chronic Kidney Disease in Subclinical Hypothyroid Populations (LP‑CKD) – A Multicenter Randomized Controlled Trial
dc.typePublication
dspace.entity.typeArticle

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