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NCT04278313 · ClinicalTrials.gov registry record · NA
Ovarian Function Following Intraovarian Injection of PRP
A NA study of Diminished Ovarian Reserve and Diminished Ovarian Reserve Due to Advanced Maternal Age, sponsored by Center for Human Reproduction.
- Active
- Registry status
- NA
- Development phase
- 90
- Enrollment target
- 1
- Study location
NCT04278313 is a NA study of Diminished Ovarian Reserve and Diminished Ovarian Reserve Due to Advanced Maternal Age that is active but no longer recruiting, run by Center for Human Reproduction. The registered enrollment target is 90 participants. The trial reports 1 study location across 1 state.
The verdict
NCT04278313, a NA study of Diminished Ovarian Reserve and Diminished Ovarian Reserve Due to Advanced Maternal Age, is active but no longer recruiting, sponsored by Center for Human Reproduction.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 90 participants
- Enrollment target
- 1
- Study location
Study Summary
Consenting women with evidence of poor ovarian reserve will be randomly assigned to treatment with either Platelet Rich Plasma (PRP) or Platelet Poor Plasma (PPP).
Conditions Studied
Interventions
- PROCEDURE PRP - Platelet Rich Plasma
- PROCEDURE PPP - Platelet Poor Plasma
Study Locations (1)
New York
- Center for Human Reproduction - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2020-02-24 |
| Est. Completion | 2026-12-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04278313
The ClinicalTrials.gov registry entry for NCT04278313 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Center for Human Reproduction, which has 8 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Diminished Ovarian Reserve appearing as the primary indexed condition, and to 2 interventions - of which PRP - Platelet Rich Plasma is the first listed.
NCT04278313 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT04278313 about?
NCT04278313 is a clinical study titled "Ovarian Function Following Intraovarian Injection of PRP". Consenting women with evidence of poor ovarian reserve will be randomly assigned to treatment with either Platelet Rich Plasma (PRP) or Platelet Poor Plasma (PPP).
What is the current status of trial NCT04278313?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2020-02-24. Estimated completion is 2026-12-31.
What conditions does trial NCT04278313 study?
This clinical trial studies the following conditions: Diminished Ovarian Reserve, Diminished Ovarian Reserve Due to Advanced Maternal Age.
What interventions are being tested in trial NCT04278313?
The interventions under investigation include: PRP - Platelet Rich Plasma (PROCEDURE), PPP - Platelet Poor Plasma (PROCEDURE).
Who is sponsoring clinical trial NCT04278313?
This trial is sponsored by Center for Human Reproduction, which has 8 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04278313 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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