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NCT03594201

A Retrospective Study on the Effect of Male Progressive Sperm Count After Semen Pretreatment on ICSI Fertilization Outcome

Completed Last updated 21 May 2019
What this trial tests

trial testing semen pretreatment in Sperm Count, Low in 12,215 participants. Completed in 3 January 2018.

Timeline
1 January 2016
Primary endpoint
31 December 2017
3 January 2018

Quick facts

Lead sponsorReproductive & Genetic Hospital of CITIC-Xiangya
StatusCompleted
Study typeOBSERVATIONAL
Enrollment12,215
Start date1 January 2016
Primary completion31 December 2017
Estimated completion3 January 2018
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Reproductive & Genetic Hospital of CITIC-Xiangya

Who can join

Eligibility, any sex, with Sperm Count, Low or Reproductive Sterility. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The investigators plan to retrospectively analyze clinical data from 14,189 fresh ICSI cycles in Reproductive and Genetic Hospital of CITIC-Xiangya from January 2016 to December 2017.The investigators will regard total progressive sperm number of 2 x 10\^6 after pretreatment as the boundary value, and will divide total progressive sperm number of 2 x 10\^6 after pretreatment into 2 x 10\^6 or higher and \< 2 x 10\^6 groups, and will further divide \< 2 x 10\^6 group into: = 0, (0,10\^6\], (10\^6, 2 x 10\^6) three groups. Propensity score matching will be used to balance the baseline data between four groups. The matching variables are age, female BMI, AFC, AMH and ICSI.

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 recruiting trials for Sperm Count, Low

Currently open trials in the same condition.

Other Reproductive & Genetic Hospital of CITIC-Xiangya trials

Trials by the same sponsor.

Verify against primary sources

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/NCT03594201.

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