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NCT04132622: LDETPI
Low Dose Euthyrox in Treatments of Paraquat Intoxication.
Phase 4 trial testing Levothyroxine Sodium in Paraquat Poisoning in 80 participants. Status unknown.
31 December 2022
Quick facts
| Lead sponsor | Second Affiliated Hospital, School of Medicine, Zhejiang University |
|---|---|
| Phase | Phase 4 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 80 |
| Start date | 1 January 2020 |
| Primary completion | 31 December 2022 |
| Estimated completion | 31 December 2023 |
Drugs / interventions tested
- Levothyroxine Sodium (LEVOTHYROXINE SODIUM) — full drug profile →
- Traditional therapy — full drug profile →
Conditions studied
- Paraquat Poisoning — all drugs for Paraquat Poisoning →
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Who can join
Eligibility, any sex, with Paraquat Poisoning. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Paraquat is a common human toxicant and accounts for 20 deaths per million persons in the world. Paraquat usually cause multiple organ dysfunction syndrome, including liver, kidney, lung and heart dysfunction. Besides, pituitary insufficiency also occurs on those patients with paraquat poisoning, which leads to multiple endocrine gland dysfunction, involving adrenal gland, thyroid and sex gland. As a result, the investigators decide to initiate the clinical trial to find whether thyroid replacement therapy can furtherly reduce the mortality, and improve patients long-term prognosis.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT04132622
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Levothyroxine Sodium
Trials testing the same drug.
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- NCT04878614 — Comparison of Levothyroxine Formulation in Hypothyroid Patients With Enteral Feeding · Phase 4 · terminated
- NCT03977207 — A Randomized Controlled Trial of Thyroid Hormone Supplementation in Hemodialysis Patients · NA · recruiting
- NCT03880578 — Quality of Life After Interventional Thyroid Treatment · completed
Other Second Affiliated Hospital, School of Medicine, Zhejiang University trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04132622 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Second Affiliated Hospital, School of Medicine, Zhejiang University
- Last refreshed: 22 October 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04132622.
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