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To check the effect of sperm freezing and warming for 3 times and there by studying the amount of healthy sperm recovered.

Impact of repeat freeze-thaw on functional and genetic integrity of sperm:comparison between vitrification and rapid freezing

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/05/019196
Enrollment
50
Registered
2019-05-16
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N461- Oligospermia

Interventions

Intervention1: Cryopreservation of sperm using Rapid freezing and Vitrification: storing sperm samples at subzero condition at -196C in liquid nitrogen for future use Control Intervention1: Cryopreser

Sponsors

Department of clinical Embryology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with Normozoospermic sample and Oligozoospermic sample according to WHO 2010 critiria are considered

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with STDs are excluded 2. Home collection samples are excluded

Design outcomes

Primary

MeasureTime frame
Optimization of sperm vitrificationTimepoint: 2 months

Secondary

MeasureTime frame
Viable, motile and morphological normal sperm after repeated freeze-thawTimepoint: 4 months

Countries

India

Contacts

Public ContactRahul

Manipal Academy of Higher Education

shweta.hegde@manipal.edu9110883847

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026