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NCT03837223
RESCUE PROTOCOL AND FRESH EMBRYO TRANSFER
trial testing GnRH agonist in GnRH Trigger and Rescue Protocol in 271 participants. Completed in 31 December 2016.
31 December 2016
Quick facts
| Lead sponsor | Istituto Clinico Humanitas |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 271 |
| Start date | 1 March 2013 |
| Primary completion | 31 December 2016 |
| Estimated completion | 31 December 2016 |
Drugs / interventions tested
- GnRH agonist — full drug profile →
Conditions studied
- GnRH Trigger and Rescue Protocol — all drugs for GnRH Trigger and Rescue Protocol →
Sponsor
Istituto Clinico Humanitas
Who can join
Adults 18 to 38, female only, with GnRH Trigger and Rescue Protocol. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Ovarian Hyperstimulation Syndrome (OHSS) is one of the most dangerous complications of Assisted Reproductive Technologies (ART) cycles. The use in clinical practice of the GnRH antagonist has made it possible to perform the trigger with GnRH analogues reducing the risk of OHSS. The trigger with analogue increases the Abortion Rate (AR) and reduces the Ongoing Pregnancy Rate (OPR), because the luteal phase in these cycles is particularly deficient. To reduce this occurrence several studies have focused on the importance of support of the luteal phase. The aims of study is to evaluate OPR and AR in patients at intermediate risk of OHSS (\<18 recovered oocytes) which performed GnRH trigger and rescue protocol.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03837223
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of GnRH agonist
Trials testing the same drug.
- NCT07269392 — Dual Trigger With HCG and GnRH Agonist on Thawed Modified Natural Cycle Embryo Transfer · Phase 4 · not yet recruiting
- NCT05838105 — Two Different Types of Luteal Phase Support in Natural Cycle Frozen Embryo Transfer and Its Effect on Pregnancy Rates · NA · unknown
- NCT04356664 — Benefit of GnRH Agonist Before Frozen Embryo Transfer in Patients With Endometriosis and/or Adenomyosis · Phase 2, PHASE3 · recruiting
- NCT05484193 — GnRH Agonist for Luteal Phase Support. · NA · unknown
- NCT04182594 — Cardiovascular Events in GnRH Agonist vs. Antagonist · Phase 2 · unknown
Other Istituto Clinico Humanitas trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03837223 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Istituto Clinico Humanitas
- Last refreshed: 12 February 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03837223.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing