Evidence map›Paper›PMID 41114999›Full record

Trial reportJAMA internal medicine2025

Effectiveness of Colchicine for the Treatment of Long COVID: A Randomized Clinical Trial.

Abhinav Bassi, Niveditha Devasenapathy, Shani S Thankachen, Arpita Ghosh, Aman Rastogi, Ritika Khan, Bijini Bahuleyan, Balaji Gummidi, Aneesh Basheer, Thekkumkara Prabhakaran Sreelal and 12 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in JAMA internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Abhinav BassiThe George Institute for Global Health India, Delhi, India.
Niveditha DevasenapathyThe George Institute for Global Health India, Delhi, India.
Shani S ThankachenThe George Institute for Global Health India, Delhi, India.
Arpita GhoshThe George Institute for Global Health India, Delhi, India.
Aman RastogiThe George Institute for Global Health India, Delhi, India.
Ritika KhanThe George Institute for Global Health India, Delhi, India.
Bijini BahuleyanThe George Institute for Global Health India, Delhi, India.
Balaji GummidiThe George Institute for Global Health India, Delhi, India.
Aneesh BasheerSRM Medical College Hospital and Research Centre, Chennai, India.
Thekkumkara Prabhakaran SreelalDepartment of Community Medicine, Dr Moopen's Medical College, Wayanad, India.
Ashfak BangiDepartment of General Medicine, Jivenrekha Multispeciality Hospital, Pune, India.
Yasmeen ShaikhDepartment of General Medicine, Jivenrekha Multispeciality Hospital, Pune, India.
Dibakar SahuDepartment of Pulmonary Medicine, Sleep and Critical Care, All India Institute of Medical Science, Raipur, India.
Vinay RathoreDepartment of Pulmonary Medicine, Sleep and Critical Care, All India Institute of Medical Science, Raipur, India.
Ashish BhallaDepartment of Internal Medicine, Postgraduate Institute of Medical Education & Research, Chandigarh, India.
Samita SamitaDepartment of Internal Medicine, Postgraduate Institute of Medical Education & Research, Chandigarh, India.
Merlin BlessanDepartment of General Medicine, Amrita Institute of Medical Science, Kochi, India.
T S DipuDepartment of General Medicine, Amrita Institute of Medical Science, Kochi, India.
Manish JainDepartment of Pulmonary Medicine, Maharaja Agrasen Hospital, Jaipur, India.
Abhishek Mukundbhai PrajapatiDepartment of Pulmonary Medicine, Shree Krishna Hospital, Pune, India.
Narendra Kuber BodheyDepartment of Radiodiagnosis, All India Institute of Medical Science, Raipur, India.
Vivekanand JhaThe George Institute for Global Health India, Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Long COVID is characterized by persistent symptoms after SARS-CoV-2 infection, with inflammation playing a key role in pathogenesis. Colchicine, an established anti-inflammatory agent, may reduce these symptoms by targeting inflammatory pathways. Objective: To evaluate the superiority of colchicine over placebo in improving functional outcome at 52 weeks from baseline. Design, Setting, and Participants: This double-blind, 1:1 randomized clinical trial recruited participants with confirmed SARS-CoV-2 infection and persistent symptoms from 8 hospitals in 6 states in India between January 2022 and July 2023. Individuals were eligible if they had functional limitation (Post-COVID-19 Functional Status scale grade 2 or more) and/or elevated inflammatory markers (high-sensitivity C-reactive protein >0.20 mg/dL and/or neutrophil to lymphocyte ratio >5). Outcomes were assessed at 12, 26, and 52 weeks after randomization. Data were analyzed from January to February 2025. Interventions: Participants were randomly assigned to receive colchicine, 0.5 mg, once or twice daily, based on body weight, or placebo for 26 weeks. Main Outcomes and Measures: The primary outcome was the change in distance walked during a 6-minute walk test from baseline to 52 weeks. Secondary outcomes included changes in inflammatory markers and patient-reported outcome measures, such as quality of life, anxiety, depression, fatigue, dyspnea, measured using validated instruments. Results: Of 346 participants included in the modified intention-to-treat analysis, 209 (60.4%) were female, 137 (39.6%) were male, and the mean (SD) age was 46 (12) years. At 52 weeks, there was no difference in mean (SD) change in 6-minute walk test distance between the colchicine and placebo groups (colchicine, 35.5 [19.76] m; placebo, 29.96 [19.83] m; mean difference, 5.59 m; 95% CI, -9.00 to 20.18; P = .45). Similar null findings were seen across all predefined outcomes, except for a small, nonclinically relevant difference in the mean (SD) ratio of forced expiratory volume in 1 second to forced vital capacity (colchicine, -0.02 [0.03]; placebo, -0.06 [0.03]; mean difference, 0.04; 95% CI, 0.02 to 0.07; P = .001). Conclusions and Relevance: In this randomized clinical trial, among adults with long COVID, colchicine did not improve functional capacity, respiratory function, or inflammatory markers. These findings underscore the need to explore alternative therapeutic approaches for long COVID. Trial Registration: Clinical Trial Registry of India: CTRI/2021/11/038234.

Indexed as

Anti-Inflammatory AgentsColchicineCOVID-19COVID-19 Drug TreatmentAdultDouble-Blind MethodFemaleHumansMaleMiddle AgedQuality of LifeSARS-CoV-2Treatment OutcomeAnti-Inflammatory AgentsColchicine

Identifiers

PMID41114999
PMCPMC13374639

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.