Trial · NCT04918524
The Clinical Features and Pregnancy Outcomes of CTD Patients
NCT04918524, Recruiting, Qilu Hospital of Shandong University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Clinical Features and Pregnancy Outcomes of CTD Patients. Trials, record NCT04918524. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04918524
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Clinical Features and Pregnancy Outcomes of CTD Patients
- NCT number
- NCT04918524
- Status
- Recruiting
- Enrollment
- 126 participants, estimated
- Lead sponsor
- Qilu Hospital of Shandong University
- Conditions
- Connective Tissue Diseases, Pregnancy Related
- Interventions
- Prednisone, Hydroxychloroquine, Aspirin, low molecular weight heparin Enoxaparin
- First posted
- 2021-06-09
- Last updated
- 2023-11-18
Source ClinicalTrials.gov
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Live birth rate | After 28 weeks of gestation | Percentage of all patients that lead to live birth after 28 weeks of gestation |
| Secondary | Early fetal loss | within 10 weeks of gestation | Spontaneous pregnancy loss within 10 weeks of gestation |
| Secondary | Late fetal loss | after 10 weeks of gestation | Spontaneous pregnancy loss after 10 weeks of gestation |
| Secondary | Stillbirth | after 20 weeks of gestation | Spontaneous pregnancy loss after 20 weeks of gestation |
| Secondary | Preterm delivery | between 28 and 37 weeks of gestation | Live birth before 37 weeks of gestation |
| Secondary | Low-weight birth | after 28 weeks of gestation | newborns with low weight (\<2500g) |
| Secondary | Premature rupture of membranes | after 28 weeks of gestation | the number of participants complicated with premature rupture of membranes |
| Secondary | Placental abruption | after 28 weeks of gestation | the number of participants complicated with placental abruption |
| Secondary | Fetal growth retardation (FGR) | after 12 weeks of gestation | weight below the 10th percentile for the gestational age |
| Secondary | Number of participants with low amniotic fluid during pregnancy | after 12 weeks of gestation | the number of participants whose B-ultrasound indicates low amniotic fluid during pregnancy |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 registered outcomesOutcomes0
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.
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 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/NCT04918524
GET https://conductscience.org/api/trials/v1/NCT04918524/registered