# A Comparison of the Microdose Leuprolide Protocol vs. Luteal Phase Ganirelix Protocol in Women Who Are or Who Are Predicted to be Low Responders

> **NCT00633555** · — · COMPLETED · sponsor: **UConn Health** · enrollment: 54 (actual)

## Conditions studied

- Infertility

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT00633555
- **Lead sponsor:** UConn Health
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2006-07
- **Primary completion:** 2010-09
- **Final completion:** 2010-09
- **Target enrollment:** 54 (ACTUAL)
- **Last updated:** 2018-05-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00633555

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00633555, "A Comparison of the Microdose Leuprolide Protocol vs. Luteal Phase Ganirelix Protocol in Women Who Are or Who Are Predicted to be Low Responders". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT00633555. Licensed CC0.

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