Trial · NCT00702806
Investigate Dose of Org 36286 to Initiate Multiple Follicular Growth in a Controlled Ovarian Hyperstimulation Protocol for IVF or IVF/ICSI (P07015)
NCT00702806, Phase 2, Completed, Organon and Co
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Investigate Dose of Org 36286 to Initiate Multiple Follicular Growth in a Controlled Ovarian Hyperstimulation Protocol for IVF or IVF/ICSI (P07015). Trials, record NCT00702806. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00702806
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Investigate Dose of Org 36286 to Initiate Multiple Follicular Growth in a Controlled Ovarian Hyperstimulation Protocol for IVF or IVF/ICSI (P07015)
- NCT number
- NCT00702806
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 99 participants, actual
- Lead sponsor
- Organon and Co
- Conditions
- Infertility, In Vitro Fertilization
- Interventions
- Org 36286, Puregon®, Orgalutran®, Pregnyl®
- First posted
- 2008-06-20
- Last updated
- 2024-08-15
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Median Puregon® Dose (IU) Required To Reach Criteria for Administration of Human Chorionic Gonadotropin (hCG) For Induction of Final Oocyte Maturation | Day 8 Up to End of Menstrual Cycle | |
| Secondary | Number of Participants Experiencing Cancellation of Menstrual Cycle | Up to End of Menstrual Cycle | |
| Secondary | Number of Cumulus-Oocyte-Complexes Experienced By Participants During One Menstrual Cycle | Up to End of Menstrual Cycle | |
| Secondary | Number of Good Quality Embryos Obtained | Up to One Menstrual Cycle | |
| Secondary | Number of Participants With Ongoing Pregnancies | Up to 10 Weeks Following hCG Administration | |
| Secondary | Number of Participants With Anti-Org 36286 Antibodies | Up to 2 Weeks Following Embryo Transfer | |
| Secondary | Number of Participants With Abnormal Laboratory Findings | Up to 2 Weeks Following Embryo Transfer | |
| Secondary | Number of Participants With Abnormal Vital Signs | Up to 2 Weeks Following Embryo Transfer | |
| Secondary | Number of Participants With Serious Adverse Events (SAEs) | Up to 2 Weeks Following Embryo Transfer |
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 |
|---|---|
| 15126522 | RESULT |
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/NCT00702806
GET https://conductscience.org/api/trials/v1/NCT00702806/registered