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Clinical Trials/ChiCTR-DDD-17010376
ChiCTR-DDD-17010376Active, not recruiting诊断试验新技术临床试验

无创胚胎染色体筛查技术评估胚胎染色体整倍性的多中心临床研究

江苏省重点研发计划12 sites in 1 countryStarted: January 1, 2017Last updated:

Trial Snapshot

Phase
诊断试验新技术临床试验
Status
Active, not recruiting
Sponsor
Locations
12
Primary Endpoint
敏感度、特异度、准确性

Study Overview

Brief Summary

寻求一种无创的胚胎染色体筛查技术替代现有的有创活检方法

Study Design

Study Type
诊断试验
Primary Purpose
诊断试验诊断准确性

Eligibility Criteria

Ages
20 to 45 (—)
Sex
Female

Inclusion Criteria

  • 1)ICSI 治疗周期中废弃胚胎或 PGS、PGD 胚胎;2)愿意依从本研究方案签署知情同意书。

Exclusion Criteria

  • 有辅助生殖技术治疗禁忌症的患者。

Outcomes

Primary Outcomes

敏感度、特异度、准确性

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
江苏省重点研发计划

Study Sites (12)

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