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NCT06083727
Primary Cesarean Section in Primigravida and Muligravida in Sohag and Al Balyana Cities
trial testing rate of cesarean section in Primary Cesarean Section in 100 participants. Status unknown.
24 March 2024
Quick facts
| Lead sponsor | Sohag University |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 100 |
| Start date | 24 September 2023 |
| Primary completion | 24 March 2024 |
| Estimated completion | 24 March 2024 |
| Sites | 1 location across Egypt |
Drugs / interventions tested
- rate of cesarean section
Conditions studied
- Primary Cesarean Section — all drugs for Primary Cesarean Section →
Sponsor
Sohag University
Who can join
Adults 18 to 45, female only, with Primary Cesarean Section. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
cesarean section and vaginal delivery are two methods of delivery, cesarean section somtimes indicated for obstetrical reason but primary cesarean section especially in primigravida might have a preference of the mode of delivery
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06083727
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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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 NCT06083727 (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 Sohag University
- Last refreshed: 16 October 2023
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/NCT06083727.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing