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NCT02741141: PARTODYS
A Comparative Study of the Effect of Two Partographs on the Cesarean Section Rate in Women in Spontaneous Labour
NA trial testing New partograph based on the studies of Neal and Lowe in Dystocia in 633 participants. Terminated before completion.
7 October 2019
Quick facts
| Lead sponsor | University Hospital, Strasbourg, France |
|---|---|
| Phase | NA |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | diagnostic |
| Enrollment | 633 |
| Start date | 21 September 2016 |
| Primary completion | 7 October 2019 |
| Estimated completion | 7 October 2019 |
| Sites | 1 location across France |
Drugs / interventions tested
- New partograph based on the studies of Neal and Lowe
- Classical partograph
Conditions studied
- Dystocia — all drugs for Dystocia →
Sponsor
University Hospital, Strasbourg, France
Who can join
18 and older, any sex, with Dystocia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
In the 2010-french perinatal survey, the overall cesarean section (CS) rate during labour was 21 % and 16% to 38% in case of dystocia. The definition of " dystocia " is traditionally based on the research led by Friedman in the 1950's on a restricted population sample. Several studies over the last years seem to indicate that the different phases of labour are longer than originally described by Friedman. Our current hypothesis is that the application of a new definition of dystocia would enable a more appropriate management of labour.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Effect of partograph use on outcomes for women in spontaneous labour at term and their babies.
Lavender T, Cuthbert A, Smyth RM. · · 2018 · cited 47× · PMID 30080256 · DOI 10.1002/14651858.cd005461.pub5
Verify or expand the search:
- PubMed search for NCT02741141
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT02741141 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University Hospital, Strasbourg, France
- Last refreshed: 14 October 2021
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/NCT02741141.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing