Trial · NCT00589329
Antibiotics and the Prolongation of Pregnancy in Preterm Labor With an Advanced Cervical Exam
NCT00589329, Not applicable, Terminated, MetroHealth Medical Center; results first posted 2019-09-04
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Antibiotics and the Prolongation of Pregnancy in Preterm Labor With an Advanced Cervical Exam. Trials, record NCT00589329. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00589329
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Antibiotics and the Prolongation of Pregnancy in Preterm Labor With an Advanced Cervical Exam
- NCT number
- NCT00589329
- Status
- Terminated
- Phases
- Not applicable
- Enrollment
- 20 participants, actual
- Lead sponsor
- MetroHealth Medical Center
- Conditions
- Length of Pregnancy Prolongation in Hours
- Interventions
- erythromycin and metronidazole (antibiotics), placebo
- First posted
- 2008-01-09
- Last updated
- 2019-09-04
- Results first posted
- 2019-09-04
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Length of Pregnancy Prolongation | Measured from randomization to delivery in hours | The length of time (in hours) from initiation of therapy to delivery will establish the latency |
| Secondary | Respiratory Distress | newborn nursery | Respiratory distress will be defined by the clinical record documentation of the neonatal team. |
Source ClinicalTrials.gov
Outcomes2
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Length of Pregnancy Prolongation | Measured from randomization to delivery in hours | hours | MEAN | |
| SECONDARY | Respiratory Distress | newborn nursery | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.gov
Results by group4
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Length of Pregnancy Prolongation | Group A | 4 | Full Range 0 to 36 | hours | |
| Length of Pregnancy Prolongation | Group B | 4 | Full Range 1 to 38 | hours | |
| Respiratory Distress | Group A | 2 | Participants | ||
| Respiratory Distress | Group B | 1 | Participants |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Group A | 10 | |
| Overall Study | STARTED | Group B | 10 | |
| Overall Study | COMPLETED | Group A | 10 | |
| Overall Study | COMPLETED | Group B | 10 | |
| Overall Study | NOT COMPLETED | Group A | 0 | |
| Overall Study | NOT COMPLETED | Group B | 0 |
Source ClinicalTrials.gov
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 totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Group A | ||
| Total, all-cause mortality | Group B | ||
| Total, other adverse events | Group A | 0 | 10 |
| Total, other adverse events | Group B | 0 | 10 |
| Total, serious adverse events | Group A | 0 | 10 |
| Total, serious adverse events | Group B | 0 | 10 |
Source ClinicalTrials.gov
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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 comparisons2
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Group A vs Group B: Respiratory Distress | Trial comparisons |
| Group A vs Group B: serious adverse events | Trial comparisons |
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/NCT00589329
GET https://conductscience.org/api/trials/v1/NCT00589329/registered