Trial · NCT01869556
Comparison of IV Ergonovine With IM Carboprost, With Oxytocin IV, During Cesarean Section for Failure to Progress
NCT01869556, Not applicable, Completed, Samuel Lunenfeld Research Institute, Mount Sinai Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of IV Ergonovine With IM Carboprost, With Oxytocin IV, During Cesarean Section for Failure to Progress. Trials, record NCT01869556. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01869556
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of IV Ergonovine With IM Carboprost, With Oxytocin IV, During Cesarean Section for Failure to Progress
- NCT number
- NCT01869556
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 105 participants, actual
- Lead sponsor
- Samuel Lunenfeld Research Institute, Mount Sinai Hospital
- Conditions
- Postpartum Hemorrhage
- Interventions
- Oxytocin, Ergot, Carboprost
- First posted
- 2013-06-05
- Last updated
- 2020-09-24
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Need for additional uterotonics intraoperatively | 1 hour | Need for additional uterotonics intraoperatively if requested by the surgeon, YES or NO |
| Secondary | Effectiveness of uterine contraction | 10 min | Adequate/inadequate uterine tone at 3,5 \& 10 min |
| Secondary | Need for blood transfusion | 24 hours | Any blood products administered |
| Secondary | Vital signs | 2 hours | In the OR, heart rate, blood pressure, and oxygen saturation will be measured and looked at for abnormalities |
| Secondary | Side effects | 24 hours | The presence of nausea, vomiting,other dysrhythmias, chest pain, headache, bronchospasm and any others will be recorded. |
| Secondary | Estimated blood loss | 48 hours | calculated blood loss = EBV (Pre-op Htc-Post-op Htc) EBV (estimated blood volume, mL)=patient's weight in kg x 85 |
| Secondary | Need for additional uterotonics or interventions post-operatively | 24 hours | Need for additional uterotonics or interventions post-operatively up to 24 hours post-partum |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 33543897 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT01869556
GET https://conductscience.org/api/trials/v1/NCT01869556/registered