ORPHA:95486
Premature closure of the arterial duct
Also known as: Premature closure of the patent ductus arteriosus
Publications
29
36.4th percentile
Trials
0
Interventional, condition-specific
Researchers
138
Distinct authors in sample
Gene link
—
Readiness
1/6
Stages with a signal
Clinical definition (Orphanet)
Premature closure of the arterial duct is a rare arterial duct anomaly, defined as a significant constriction or closure of the fetal arterial duct in the absence of structural heart defects with pathognomonic features of increased right ventricular afterload, tricuspid regurgitation and, consequently, right atrial dilation and right ventricular hypertrophy. The severity of symptoms is related to the degree and rate of ductal constriction and ranges from mild postnatal respiratory distress to development of ventricular failure with fetal hydrops and intrauterine death or severe cardiopulmonary compromise in the postnatal period. It may be associated with a exposure to cyclooxygenase inhibitors or corticosteroids.
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0019823
- UMLS:C3532264
Additional Mondo synonyms (1)
premature closure of the patent ductus arteriosus
Research stages
Trial readiness signals
Where this condition sits on an open-data research pipeline — not how close a treatment is, and not medical advice. Empty stages often mean “not in these databases under this Mondo ID,” not “impossible.”
1/6 stages with a signal
Research-stage checklist from open sources (GenCC, literature, Monarch when enriched, ClinicalTrials.gov). Not a prognosis or care recommendation.
- Gene identifiedNot found
No GenCC disease–gene assertion in this build
- LiteraturePresent
29 matched papers (19 in last 10 years) Source
- Phenotype characterisedNot checked
Not yet enriched from Monarch / HPO
- Animal modelNot checked
Not yet enriched from Monarch / Alliance
- Orphan designationNot checked
FDA/EMA orphan-drug designation not enriched yet
- Interventional trialNot found
No matched interventional trial under our ClinicalTrials.gov rules
Biology
Genes and phenotypes
Gene–disease validity from GenCC, plus phenotypes and animal models joined from Monarch Initiative via Mondo ID — not a clinical diagnosis aid.
Do we know what causes it?
Not yet — the cause hasn't been pinned down in GenCC.
No strong gene–disease assertion joined for this Orphanet entity.
Phenotypes (Monarch / HPO)
Not enriched in this build — Monarch phenotype joins were not run for this record.
Animal models (Monarch / Alliance)
Not enriched in this build.
Literature
Is anyone studying this?
29
29 papers have ever been published on this condition (under this name). For scale, breast cancer has over 700,000. Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=5449) is 41.
29 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 41 (publications denominator n=5449).
19 in the last 10 years · high confidence · 36.4th percentile (publications denominator)
Phrase hits: 29 · MeSH hits: 0
Who's working on it?
138
Distinct author names in 29 sampled papers — named people below.
Who's working on it?
No interventional trial matched this name; these authors publish on it in the sampled literature — a practical starting point for contact.
- 01Aalishahi T1 paper · 2022
Student of Midwifery Master of Science, Student Research Committee, School of Nursing and Midwifery, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
Papers in Europe PMC - 02Ahmed F1 paper · 2023
Department of Internal Medicine, Cleveland Clinic, Cleveland, Ohio, USA.
Papers in Europe PMC - 03Alexopoulos D1 paper · 2019
Department of Neurology, Washington University, Saint Louis, Missouri, United States of America.
Papers in Europe PMC - 04Ali S1 paper · 2022
Pediatrics, Stollery Children's Hospital, Edmonton, Alberta, Canada.
Papers in Europe PMC - 05Avasthi A1 paper · 2015
Department of Psychiatry, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Papers in Europe PMC - 06Bacci C1 paper · 2021
Dental Clinic, Department of Neuroscience, University of Padua, 35129 Padua, Italy.
Papers in Europe PMC - 07Bandiera M1 paper · 2021
Dental Clinic, Department of Neuroscience, University of Padua, 35129 Padua, Italy.
Papers in Europe PMC - 08Beattie K1 paper · 2022
Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Papers in Europe PMC - 09Beeker N1 paper · 2024
UPR7323 "Pharmacology and Drug Evaluatioán in Children and Pregnant Women", Université Paris Cité, Paris, Île-de-France, France.
Papers in Europe PMC - 10Berglund F1 paper · 2023
Department of Internal Medicine, Cleveland Clinic, Cleveland, Ohio, USA.
Papers in Europe PMC
Clinical research
Is a treatment being tested?
0
interventional trials for this specific condition
No interventional trial testing a treatment matched this specific condition name on ClinicalTrials.gov (observational studies and pan-disease registries are listed separately when present).
Data as of 27 July 2026
No matched interventional trials. This is true for 73% of diseases in the trials denominator (5114 of 7003). Here are the researchers publishing on it.
high confidence · 36.5th percentile (trials denominator)
Recruiting interventional trials
From the matched ClinicalTrials.gov set
No interventional trial testing a treatment was found for this specific condition name on ClinicalTrials.gov.
See who's working on it — people publishing on this disease are often the practical next contact when no trial is listed.
Where to find support
We do not yet link condition-specific patient organisations. These umbrella groups support undiagnosed and ultra-rare families:
India — NPRD
Last verified 2026-07-26This ORPHAcode is not on our curated NPRD list (direct or Mondo-parent match). That does not decide clinical eligibility; families in India should ask a notified Centre of Excellence about current coverage.
Hand-curated for this project. ORPHAcode mappings are best-effort and may be incomplete or imprecise for umbrella categories. Parent (Mondo) matches mean the policy lists a broader category — confirm eligibility with a Centre of Excellence. Financial entitlements summarised from public policy statements and may change. This is not official government guidance.
How we counted this
Europe PMC query (preferred label + any corrected label + Orphanet and Mondo exact synonyms, stoplisted; unioned with resolved MeSH labels when available). UMLS / OMIM / NCIT cross-references are stored on the overview but are not added to the query string.
"Premature closure of the arterial duct" OR "Premature closure of arterial duct" OR "Premature closure of the patent ductus arteriosus" OR "Premature closure of patent ductus arteriosus"
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Premature closure of the arterial duct" OR "Premature closure of arterial duct" OR "Premature closure of the patent ductus arteriosus" OR "Premature closure of patent ductus arteriosus"
Study-type breakdown: 0 interventional · 0 observational · 0 expanded access. Only interventional studies enter the trial headline.
Query health: ok — strategies attempted: phrase; with hits: phrase
Run this search on ClinicalTrials.gov
Confidence reasoning
- Preferred label is multi-word and distinctive
- No synonyms dropped by stoplist
- No label/synonym collisions with other diseases in this corpus
Ingested 2026-07-27T04:45:05.454Z