Clinical trial · Interventional
GnRH Antagonist Pre-treatment in the Early Follicular Phase for Resolution of a Baseline Functional Ovarian Cyst
GnRH Antagonist Pre-treatment in the Early Follicular Phase for Resolution of a Baseline Functional Ovarian Cyst - A Proof-of-concept Pilot Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In this study we would like to examine the effect of GnRH antagonist administration at the beginning of the follicular phase in patient presenting with a simple ovarian cyst 25-50 mm. The aim of this intervention is to allow a spontaneous regression of the ovarian cyst (if in nature) while ensuring a pituitary downregulation to prevent the beginning of a leading follicle recruitment. As previous studies using GnRH antagonist pre-treatment prior to GT initiation for other purposes demonstrated positive results (including different patient population) , no deleterious effects are expected.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| IVF | — | UNRESOLVED | — |
| Ovarian Cysts | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cetrorelix Acetate, Ganerelix Acetate | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Participants
- description
- Patients will start GnRH antagonist injections \[Cetrotide (cetrolix) or Orgalutran (ganirelix) - depending on their primary prescription\] for 3-6 days
- interventionNames
- Drug: Cetrorelix Acetate, Ganerelix Acetate
Primary outcomes (2)
- measure
- Cyst resolution
- timeFrame
- 2 years
- description
- Number of participants with a resolution/decrease in size of the cystic structure following GnRH antagonist.
- measure
- Number of oocytes retrieved
- timeFrame
- 2 years
- description
- cycle outcome - number of oocytes retrieved, of participants following the administration of the GnRH antagonist
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 45 Years
Show eligibility criteria text
Inclusion Criteria: 1. Antagonist protocol. 2. Presentation for cycle initiation on day 2-3 of the menstrual cycle with a simple ovarian cyst \>25 mm and \< 50mm, and estradiol levels \< 220 pmol/L. Exclusion Criteria: 1. Inability to provide informed consent. 2. Oocyte donor
References
Publications (0)
Data not yet available