Trial · NCT03921710
CAPA-IVM Versus STANDARD IVM
NCT03921710, Not applicable, Completed, Mỹ Đức Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. CAPA-IVM Versus STANDARD IVM. Trials, record NCT03921710. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03921710
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- CAPA-IVM Versus STANDARD IVM
- NCT number
- NCT03921710
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 80 participants, actual
- Lead sponsor
- Mỹ Đức Hospital
- Conditions
- Infertility, Female
- Interventions
- CAPA-IVM, Standard-IVM
- First posted
- 2019-04-19
- Last updated
- 2019-04-23
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Live birth rate | At least 24 weeks of gestation up to the time of delivery | Live birth is defined as the birth of at least one newborn after 24 weeks' gestation that exhibits any sign of life (twin will be a single count). For the timing of this occur, ongoing pregnancy will be used, i.e. ongoing pregnancy at 12 weeks will be used in calculations, conditional on the fact that this ongoing pregnancy results in live birth. |
| Secondary | Ongoing pregnancy rate | At a minimum of 12 weeks from the beginning of the last menstrual cycle | Pregnancy with detectable heart rate at 12 weeks' gestation |
| Secondary | Clinical pregnancy rate | At a minimum of 12 weeks from the beginning of the last menstrual cycle | Pregnancy with detectable gestational sac at 7 weeks' gestation |
| Secondary | Number of oocytes retrieved | Maximum at 30 minutes after oocyte retrieval procedure | The number of oocyte identified after oocyte retrieval |
| Secondary | Oocyte maturation rate | After at least 30 hours of maturation culture | Rate of mature oocytes on culture oocytes |
| Secondary | Number of fertilized oocytes | 16-18 hours after intra-cytoplasmic sperm injection | Number of fertilized oocyte after sperm insemination |
| Secondary | Number of embryos | At least 3 days after intra-cytoplasmic sperm injection | Number of cleavage embryos obtained |
| Secondary | Number of good quality embryos | At least 3 days after intra-cytoplasmic sperm injection | Number of good cleavage embryos obtained |
| Secondary | Number of embryos frozen | At least 3 days after intra-cytoplasmic sperm injection | Number of cleavage embryos frozen |
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.
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/NCT03921710
GET https://conductscience.org/api/trials/v1/NCT03921710/registered