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NCT04046510
Comparaison of 3 Protocols of Ocytocin Administration in C Section
NA trial testing Ocytocin in Cesarean Section Complications in 180 participants. Completed in 31 July 2019.
31 March 2019
Quick facts
| Lead sponsor | Mongi Slim Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | prevention |
| Enrollment | 180 |
| Start date | 1 September 2018 |
| Primary completion | 31 March 2019 |
| Estimated completion | 31 July 2019 |
| Sites | 1 location across Tunisia |
Drugs / interventions tested
- Ocytocin — full drug profile →
Conditions studied
- Cesarean Section Complications — all drugs for Cesarean Section Complications →
- Oxytocin Adverse Reaction — all drugs for Oxytocin Adverse Reaction →
Sponsor
Mongi Slim Hospital
Who can join
18 and older, female only, with Cesarean Section Complications or Oxytocin Adverse Reaction. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study aimed to compare 3 doses of ocytocin in bolus injection and contnious perfusion during C section. these doses determined by: high, intermediate and low doses, were administred to parturients during elective or urgent C section under spinal anesthesia
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04046510
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Cesarean Section Complications
Currently open trials in the same condition.
- NCT07278037 — Trends in the Administration of Tranexamic Acid for Postpartum Hemorrhage · recruiting
- NCT05224726 — Platelet Rich Plasma for Uterine Scar · NA · recruiting
- NCT07130747 — Effect of Myofascial Release Versus Deep Friction Massage on Abdominal Recovery and Scar After Cesarean Section · NA · recruiting
- NCT05791630 — The Norwegian World Health Organisation Labour Care Guide Trial (NORWEL) · NA · recruiting
- NCT07049705 — Factors Influencing Bradycardia During Spinal Anesthesia in Obstetric Patients Undergoing Cesarean Section · active not recruiting
Other Mongi Slim Hospital trials
Trials by the same sponsor.
- NCT06511427 — Difficult Airways Scores Validation Difficult Laryngoscopy and Mask Ventilation: Prospective and Evaluative Study · not yet recruiting
- NCT06676865 — Preoperative Prediction of Difficult Laryngoscopy in Diabetic Patients: Importance of the Palm Print Test · completed
- NCT06444737 — Contribution of Ondansetron to Preventing Post-Dural Puncture Headaches Following Spinal Anesthesia · NA · recruiting
- NCT06203353 — Evaluation of the Diaphragm Performance During Weaning From Mechanical Ventilation · unknown
- NCT06622096 — Evaluation of Lab Exams Accuracy in the Intensive Care Unit · completed
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 NCT04046510 (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 Mongi Slim Hospital
- Last refreshed: 6 August 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/NCT04046510.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing