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NCT02200952

Luteal Phase Supplementation With Recombinant LH After GnRh Agonist Oocytes Triggering in Women at Risk of OHSS

Completed Last updated 24 November 2020
What this trial tests

trial testing recombinant LH in Ovarian Hyperstimulation Syndrome in 16 participants. Completed in 30 June 2014.

Timeline
30 June 2013
Primary endpoint
30 June 2014
30 June 2014

Quick facts

Lead sponsorSan Carlo Public Hospital, Potenza, Italy
StatusCompleted
Study typeOBSERVATIONAL
Enrollment16
Start date30 June 2013
Primary completion30 June 2014
Estimated completion30 June 2014
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

San Carlo Public Hospital, Potenza, Italy

Who can join

Adults 18 to 43, female only, with Ovarian Hyperstimulation Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to prove that luteal phase supplementation with recombinant LH can solve the luteal phase deficiency after Gnrh agonist oocytes triggering in women at risk of OHSS

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other San Carlo Public Hospital, Potenza, Italy trials

Trials by the same sponsor.

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Data sources for this page

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/NCT02200952.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing